Copper‐Catalyzed Azide–Ynamide Cyclization to Generate α‐Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N‐Heterocycles
Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycl...
Saved in:
Published in | Angewandte Chemie International Edition Vol. 59; no. 41; pp. 17984 - 17990 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
05.10.2020
Wiley Subscription Services, Inc |
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX‐Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide–alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations.
An efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is disclosed, enabling divergent synthesis of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities, representing the first generation of α‐imino copper carbenes directly from alkynes. The asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities. |
---|---|
AbstractList | Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via α-imino copper carbene intermediates is reported, representing the first generation of α-imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N-heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide-ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX-Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide-alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations.Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via α-imino copper carbene intermediates is reported, representing the first generation of α-imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N-heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide-ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX-Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide-alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations. Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX‐Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide–alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations. An efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is disclosed, enabling divergent synthesis of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities, representing the first generation of α‐imino copper carbenes directly from alkynes. The asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities. Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX‐Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide–alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations. Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via alpha-imino copper carbene intermediates is reported, representing the first generation of alpha-imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N-heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide-ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX-Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide-alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations. |
Author | Wang, Ze‐Shu Liu, Rai‐Shung Zhai, Tong‐Yi Chen, Yang‐Bo Liu, Xin Deng, Chao Luo, Chen Zhang, Yi‐Ping Ye, Long‐Wu |
Author_xml | – sequence: 1 givenname: Xin surname: Liu fullname: Liu, Xin organization: Xiamen University – sequence: 2 givenname: Ze‐Shu surname: Wang fullname: Wang, Ze‐Shu organization: Xiamen University – sequence: 3 givenname: Tong‐Yi surname: Zhai fullname: Zhai, Tong‐Yi organization: Xiamen University – sequence: 4 givenname: Chen surname: Luo fullname: Luo, Chen organization: Xiamen University – sequence: 5 givenname: Yi‐Ping surname: Zhang fullname: Zhang, Yi‐Ping organization: Xiamen University – sequence: 6 givenname: Yang‐Bo surname: Chen fullname: Chen, Yang‐Bo organization: Xiamen University – sequence: 7 givenname: Chao surname: Deng fullname: Deng, Chao email: chaodeng@njau.edu.cn organization: Nanjing Agricultural University – sequence: 8 givenname: Rai‐Shung surname: Liu fullname: Liu, Rai‐Shung organization: National Tsing-Hua University – sequence: 9 givenname: Long‐Wu orcidid: 0000-0003-3108-2611 surname: Ye fullname: Ye, Long‐Wu email: longwuye@xmu.edu.cn organization: Chinese Academy of Sciences |
BookMark | eNqNkstu1DAUhi1URC-wZW2JDRLK4EscJ-xGYWhHqgoLWLCKHOcEucrYg-0pyqz6CEgs-xR9ER6iT4LDjIpUCcHKRz7f9x_LOsfowDoLCD2nZEYJYa-VNTBjhBEiGSkeoSMqGM24lPwg1TnnmSwFPUTHIVwmvixJ8QQdclYwynl5hG5qt16Dv7v-XquohnELHZ5vTQd31z8-W7VKFa5HPZitisZZHB0-BQteRcA_b5O2XBnr8C4F18q3qRve4LfmCvwXsBEr2-GFVTbpAQbQMXXwXGsIYUr74IZRTwM0vkhxZxDBu-kCwlP0uFdDgGf78wR9erf4WJ9l5-9Pl_X8PNNckCJrO0ZbKkgPWvZtS1uuNFSSCFboqsyBd1XRAxdSyV5qTovUZ0XJgUgKuiX8BL3c5a69-7qBEJuVCRqGQVlwm9CwnBEqhMiLhL54gF66jbfpdYnKC0lLXslElTvqG7SuD9qA1dCsvVkpPzaEECGqqsplqgitTfz9tbXb2JjUV_-vJnq2o7V3IXjo70lKmmk_mmk_mvv9SEL-QND78dErM_xdq_avMgOM_xjSzC-Wiz_uLxYh1MM |
CitedBy_id | crossref_primary_10_1016_j_ccr_2021_214131 crossref_primary_10_1002_anie_202201436 crossref_primary_10_1039_D4CS01329H crossref_primary_10_1002_anie_202115554 crossref_primary_10_1002_tcr_202100159 crossref_primary_10_1002_slct_202301685 crossref_primary_10_1007_s11426_021_1069_7 crossref_primary_10_1021_acscatal_1c00461 crossref_primary_10_1002_adsc_202101412 crossref_primary_10_1016_j_cclet_2024_109895 crossref_primary_10_1021_acs_jmedchem_1c01411 crossref_primary_10_1021_acs_orglett_1c03830 crossref_primary_10_3390_molecules26082318 crossref_primary_10_1002_anie_202216923 crossref_primary_10_1007_s11426_024_1990_y crossref_primary_10_1016_j_cclet_2022_06_070 crossref_primary_10_1021_acs_joc_4c02704 crossref_primary_10_1021_acs_inorgchem_1c01623 crossref_primary_10_1039_D2QO00457G crossref_primary_10_1055_a_1957_4104 crossref_primary_10_1038_s41467_022_30001_7 crossref_primary_10_1039_D2SC06152J crossref_primary_10_1126_sciadv_adg4648 crossref_primary_10_1039_D1OB01846A crossref_primary_10_1039_D2QO01786E crossref_primary_10_1002_ange_202115554 crossref_primary_10_1038_s41467_023_36190_z crossref_primary_10_1016_j_xcrp_2021_100448 crossref_primary_10_1038_s42004_023_00999_y crossref_primary_10_1002_ange_202204603 crossref_primary_10_1039_D4CC01645A crossref_primary_10_1039_D1QO00026H crossref_primary_10_1016_j_tetlet_2023_154607 crossref_primary_10_1002_adsc_202401584 crossref_primary_10_1021_acs_orglett_4c01013 crossref_primary_10_1002_anie_202210637 crossref_primary_10_1002_ange_202113464 crossref_primary_10_1007_s11426_022_1536_9 crossref_primary_10_1002_cjoc_202300498 crossref_primary_10_1039_D3SC01880F crossref_primary_10_1021_acs_orglett_4c04444 crossref_primary_10_1039_D3CC04817A crossref_primary_10_1055_a_2341_9185 crossref_primary_10_1002_anie_202204603 crossref_primary_10_1021_acs_joc_1c02849 crossref_primary_10_1002_ange_202210637 crossref_primary_10_1016_j_tet_2021_132238 crossref_primary_10_6023_cjoc202201006 crossref_primary_10_1039_D1OB02091A crossref_primary_10_1021_acs_orglett_2c00197 crossref_primary_10_1002_adsc_202300002 crossref_primary_10_1002_adsc_202300241 crossref_primary_10_1021_acs_orglett_1c03852 crossref_primary_10_1021_acs_orglett_3c01693 crossref_primary_10_6023_cjoc202211046 crossref_primary_10_1039_D2QO00685E crossref_primary_10_1055_a_2119_5390 crossref_primary_10_1039_D3OB00843F crossref_primary_10_1021_acs_joc_2c01684 crossref_primary_10_1002_anie_202303670 crossref_primary_10_1021_acscatal_0c04180 crossref_primary_10_1021_acs_orglett_3c00319 crossref_primary_10_1002_anie_202113464 crossref_primary_10_1021_acscatal_3c01680 crossref_primary_10_1002_ejoc_202101269 crossref_primary_10_1002_chem_202302821 crossref_primary_10_1021_acs_joc_4c00199 crossref_primary_10_1039_D0CS00474J crossref_primary_10_1002_ange_202201436 crossref_primary_10_1021_acs_orglett_1c03092 crossref_primary_10_1039_D1SC02773E crossref_primary_10_1016_j_jscs_2023_101658 crossref_primary_10_1021_acscatal_0c04786 crossref_primary_10_1021_acs_orglett_4c01679 crossref_primary_10_1039_D2QO00123C crossref_primary_10_1021_acs_orglett_3c00434 crossref_primary_10_1002_ange_202303670 crossref_primary_10_1021_jacs_0c10682 crossref_primary_10_3390_molecules28093691 crossref_primary_10_1002_ange_202216923 |
Cites_doi | 10.1002/ange.201103563 10.1002/ange.201102707 10.1002/anie.200905817 10.1021/ol5012604 10.1039/C5CS00887E 10.1021/ja053804t 10.1021/acs.orglett.9b01074 10.1002/adsc.201801425 10.1039/C4CS00304G 10.1002/ange.201908495 10.1002/chem.201904869 10.1038/s41467-019-11245-2 10.1021/cr100003s 10.1021/jacs.9b09303 10.1021/ar4002334 10.1021/acscatal.7b01038 10.1002/anie.201508309 10.1021/ol502346d 10.1002/ange.201912334 10.1021/acschembio.6b01060 10.1021/acs.orglett.6b01503 10.1021/jo035119f 10.1021/jacs.9b13975 10.1002/anie.201606043 10.1002/ange.201610665 10.1002/ange.201802445 10.1021/ol503172h 10.1021/cr500691k 10.1021/ja908538t 10.1002/anie.201103014 10.1021/ar4001839 10.1016/j.chempr.2018.02.001 10.1002/anie.201912334 10.1021/acscatal.7b02558 10.1039/C7CC09488D 10.1002/chem.201406456 10.1021/ol4019634 10.1002/anie.201203678 10.1002/anie.201703279 10.1039/C6CC08397H 10.1002/ange.201610042 10.1039/C9SC00079H 10.1039/C6CC06864B 10.1002/ange.201508119 10.1002/anie.201004073 10.1002/anie.201700596 10.1021/ol035000t 10.1021/jacs.5b06015 10.1002/ange.200905817 10.1002/anie.201811947 10.1021/acs.orglett.6b02267 10.1021/acs.orglett.8b00939 10.1021/acs.orglett.6b01627 10.1039/C6CS00171H 10.1021/acscatal.8b03011 10.1021/ar400188g 10.1002/ange.201402470 10.1002/adsc.201800909 10.1021/acs.orglett.9b00140 10.1002/chem.201500694 10.1039/C9QO00568D 10.1021/acs.orglett.6b03752 10.1039/C6OB01965J 10.1002/ange.201811947 10.1021/ja7111788 10.1002/ange.201508309 10.1002/chem.201406318 10.1039/C9QO00243J 10.1021/ja809078d 10.1002/anie.201402470 10.1021/ol2002607 10.1002/ange.201912534 10.1039/c3cc45410j 10.1002/anie.201707423 10.1039/C0SC00375A 10.1002/ange.201606043 10.1002/anie.201610665 10.1021/jacs.0c01918 10.1039/C4SC02596B 10.1002/ange.201813143 10.1016/j.ejmech.2019.03.003 10.1021/ar400181x 10.1002/anie.201102707 10.1007/s00044-014-1243-2 10.1002/anie.201301087 10.1002/adsc.201801484 10.1002/anie.201908495 10.1039/C4SC03358B 10.1002/anie.201810369 10.1002/adsc.201600022 10.1021/acscatal.9b01851 10.1002/ajoc.201500170 10.3998/ark.5550190.0010.618 10.1002/anie.201812002 10.1002/ange.201700596 10.1021/ar400193g 10.1016/j.bmc.2009.08.057 10.1002/ange.201301087 10.1039/C8SC00232K 10.1021/ol302102h 10.1021/jo401161h 10.1002/ange.201810369 10.1002/ange.201812002 10.1039/C5CS00929D 10.1021/acs.orglett.9b01501 10.1002/anie.201103563 10.1002/ange.201103014 10.1021/ar500015k 10.1002/anie.201802445 10.1039/C9CC06652G 10.1016/j.bmcl.2007.11.064 10.1021/acs.orglett.9b01011 10.1002/ange.201707423 10.1002/ange.201203678 10.1039/C8SC03525C 10.1021/ar400174p 10.1038/s41467-017-01853-1 10.1002/anie.201813143 10.1002/anie.201912534 10.1002/anie.201610042 10.1002/ange.201703279 10.1002/anie.201508119 10.1039/C8SC00986D 10.1002/ange.201004073 10.1039/c9qo00568d 10.1039/c7cc09488d 10.1039/c0sc00375a 10.1039/c8sc00986d 10.1039/c5cs00929d 10.1039/c6ob01965j 10.1039/c9cc06652g 10.1039/c9sc00079h 10.1039/c8sc00232k 10.1039/c6cc08397h 10.1039/c4cs00304g 10.1039/c8sc03525c 10.1039/c6cs00171h 10.1039/c6cc06864b 10.1039/c5cs00887e 10.1039/c9qo00243j 10.1039/c4sc02596b 10.1039/c4sc03358b |
ContentType | Journal Article |
Copyright | 2020 Wiley‐VCH GmbH 2020 Wiley-VCH GmbH. |
Copyright_xml | – notice: 2020 Wiley‐VCH GmbH – notice: 2020 Wiley-VCH GmbH. |
DBID | AAYXX CITATION 17B 1KM 1KN AOWDO BLEPL DTL EGQ 7TM K9. 7X8 |
DOI | 10.1002/anie.202007206 |
DatabaseName | CrossRef Web of Knowledge Index Chemicus Current Chemical Reactions Web of Science - Science Citation Index Expanded - 2020 Web of Science Core Collection Science Citation Index Expanded Web of Science Primary (SCIE, SSCI & AHCI) Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic |
DatabaseTitle | CrossRef Web of Science ProQuest Health & Medical Complete (Alumni) Nucleic Acids Abstracts MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic ProQuest Health & Medical Complete (Alumni) CrossRef Web of Science |
Database_xml | – sequence: 1 dbid: 1KN name: Current Chemical Reactions url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR sourceTypes: Enrichment Source Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1521-3773 |
Edition | International ed. in English |
EndPage | 17990 |
ExternalDocumentID | 000559994700001 10_1002_anie_202007206 ANIE202007206 |
Genre | article |
GrantInformation_xml | – fundername: National Natural Science Foundation of China funderid: 21772161 and 21622204 – fundername: NSFFJ grantid: 2019J02001 – fundername: NNSFC; National Natural Science Foundation of China (NSFC) grantid: 21772161; 21622204 – fundername: Start-up Research Fund of Nanjing Agricultural University grantid: 050-804099 – fundername: NFFTBS grantid: J1310024 – fundername: Fundamental Research Funds for the Central Universities grantid: 20720202008 – fundername: Science & Technology Cooperation Program of Xiamen grantid: 3502Z20183015 – fundername: President Research Funds from Xiamen University grantid: 20720180036 – fundername: Opening Project of PCOSS, Xiamen University; Xiamen University grantid: 201909 – fundername: Bioinformatics Center of Nanjing Agricultural University – fundername: PCSIRT; Program for Changjiang Scholars & Innovative Research Team in University (PCSIRT) |
GroupedDBID | --- -DZ -~X .3N .GA 05W 0R~ 10A 1L6 1OB 1OC 1ZS 23M 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5RE 5VS 66C 6TJ 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AAHQN AAMNL AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABIJN ABLJU ABPPZ ABPVW ACAHQ ACCFJ ACCZN ACFBH ACGFS ACIWK ACNCT ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFRAH AFWVQ AFZJQ AHBTC AHMBA AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB ATUGU AUFTA AZBYB AZVAB BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BTSUX BY8 CS3 D-E D-F D0L DCZOG DPXWK DR1 DR2 DRFUL DRSTM EBS F00 F01 F04 F5P G-S G.N GNP GODZA H.T H.X HBH HGLYW HHY HHZ HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LYRES M53 MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 RYL SUPJJ TN5 UB1 UPT UQL V2E VQA W8V W99 WBFHL WBKPD WH7 WIB WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XPP XSW XV2 YZZ ZZTAW ~IA ~KM ~WT AAYXX ABDBF ABJNI AEYWJ AGHNM AGYGG CITATION 17B 1KM 1KN BLEPL DTL GROUPED_WOS_WEB_OF_SCIENCE 7TM K9. 7X8 |
ID | FETCH-LOGICAL-c3506-bd21b150fec7fbb1b3ace970526c984e3d96fe357a7f7c3163ac2683e071ecb03 |
IEDL.DBID | DR2 |
ISICitedReferencesCount | 79 |
ISICitedReferencesURI | https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000559994700001 |
ISSN | 1433-7851 1521-3773 |
IngestDate | Fri Jul 11 04:22:11 EDT 2025 Fri Jul 25 11:49:02 EDT 2025 Wed Jul 09 09:59:45 EDT 2025 Fri Aug 29 15:57:16 EDT 2025 Tue Jul 01 01:17:43 EDT 2025 Thu Apr 24 22:59:59 EDT 2025 Wed Jan 22 16:33:45 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 41 |
Keywords | 2H-AZIRINES TETHERED ALKYNES C-H ANNULATION alkynes EFFICIENT SYNTHESIS RAPID ACCESS asymmetric catalysis 2-ALKYNYL ARYLAZIDES CASCADE REACTION NUCLEOPHILIC NITRENOIDS cyclizations CYCLOADDITION heterocycles copper OXO GOLD CARBENES |
Language | English |
LinkModel | DirectLink |
LogoURL | https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg |
MergedId | FETCHMERGED-LOGICAL-c3506-bd21b150fec7fbb1b3ace970526c984e3d96fe357a7f7c3163ac2683e071ecb03 |
Notes | Dedicated to the 70th anniversary of Shanghai Institute of Organic Chemistry ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0003-3108-2611 |
PMID | 32621338 |
PQID | 2446718397 |
PQPubID | 946352 |
PageCount | 7 |
ParticipantIDs | webofscience_primary_000559994700001 webofscience_primary_000559994700001CitationCount crossref_primary_10_1002_anie_202007206 wiley_primary_10_1002_anie_202007206_ANIE202007206 proquest_miscellaneous_2420155546 proquest_journals_2446718397 crossref_citationtrail_10_1002_anie_202007206 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | October 5, 2020 |
PublicationDateYYYYMMDD | 2020-10-05 |
PublicationDate_xml | – month: 10 year: 2020 text: October 5, 2020 day: 05 |
PublicationDecade | 2020 |
PublicationPlace | WEINHEIM |
PublicationPlace_xml | – name: WEINHEIM – name: Weinheim |
PublicationTitle | Angewandte Chemie International Edition |
PublicationTitleAbbrev | ANGEW CHEM INT EDIT |
PublicationYear | 2020 |
Publisher | Wiley Wiley Subscription Services, Inc |
Publisher_xml | – name: Wiley – name: Wiley Subscription Services, Inc |
References | 2014 2014; 53 126 2017; 7 2017; 8 2019; 170 2018; 360 2019; 55 2019; 10 2020 2020; 59 132 2011; 13 2012; 14 2019; 361 2013 2013; 52 125 2018; 9 2015; 48 2018; 8 2013; 15 2018; 4 2015; 137 2019; 21 2018 2018; 57 130 2012 2012; 51 124 2015; 44 2014; 16 2010; 110 2009; vi 2003; 5 2016; 358 2016; 45 2009; 17 2019; 9 2015; 6 2015; 17 2019; 6 2015; 4 2011; 2 2013; 49 2020; 142 2008; 18 2014; 47 2016; 52 2010 2010; 49 122 2017 2017; 56 129 2009; 131 2016; 18 2019; 141 2018; 20 2016; 14 2019 2019; 58 131 2015; 24 2017; 53 2016 2016; 55 128 2015; 115 2013; 78 2005; 127 2015; 21 2017; 12 2010; 132 2003; 68 2020; 26 2017; 19 2011 2011; 50 123 2014 2018; 54 2008; 130 e_1_2_6_95_3 e_1_2_6_72_2 e_1_2_6_114_2 e_1_2_6_53_2 e_1_2_6_95_2 e_1_2_6_30_3 e_1_2_6_118_1 e_1_2_6_30_2 e_1_2_6_118_2 e_1_2_6_91_2 e_1_2_6_110_1 e_1_2_6_19_2 e_1_2_6_57_3 e_1_2_6_34_2 e_1_2_6_11_2 e_1_2_6_38_2 e_1_2_6_76_2 e_1_2_6_15_2 e_1_2_6_57_2 e_1_2_6_99_2 e_1_2_6_102_2 e_1_2_6_83_2 e_1_2_6_64_2 e_1_2_6_106_1 e_1_2_6_41_3 e_1_2_6_41_2 e_1_2_6_60_1 e_1_2_6_121_2 e_1_2_6_9_2 e_1_2_6_5_2 e_1_2_6_1_1 e_1_2_6_22_3 e_1_2_6_22_2 e_1_2_6_49_2 e_1_2_6_64_3 e_1_2_6_87_3 e_1_2_6_45_1 e_1_2_6_87_2 e_1_2_6_26_2 e_1_2_6_68_2 e_1_2_6_50_2 e_1_2_6_73_2 e_1_2_6_96_2 e_1_2_6_113_2 e_1_2_6_54_1 e_1_2_6_31_2 e_1_2_6_92_2 e_1_2_6_117_2 e_1_2_6_92_3 e_1_2_6_12_2 e_1_2_6_35_2 e_1_2_6_58_2 e_1_2_6_31_3 e_1_2_6_77_2 e_1_2_6_39_1 e_1_2_6_16_1 e_1_2_6_61_2 e_1_2_6_101_3 e_1_2_6_105_1 e_1_2_6_42_2 e_1_2_6_65_1 e_1_2_6_80_2 e_1_2_6_109_2 e_1_2_6_120_2 e_1_2_6_101_2 e_1_2_6_6_3 e_1_2_6_6_2 e_1_2_6_23_3 e_1_2_6_46_3 e_1_2_6_109_3 e_1_2_6_23_2 e_1_2_6_2_2 e_1_2_6_27_2 e_1_2_6_88_1 e_1_2_6_69_1 e_1_2_6_46_2 e_1_2_6_97_1 e_1_2_6_51_2 e_1_2_6_74_2 e_1_2_6_116_2 e_1_2_6_93_2 e_1_2_6_70_2 e_1_2_6_112_2 e_1_2_6_13_2 e_1_2_6_59_2 e_1_2_6_59_3 e_1_2_6_32_2 e_1_2_6_55_1 e_1_2_6_78_1 e_1_2_6_17_2 e_1_2_6_36_2 e_1_2_6_62_2 e_1_2_6_104_1 e_1_2_6_85_2 e_1_2_6_20_1 e_1_2_6_108_2 e_1_2_6_81_2 e_1_2_6_108_3 e_1_2_6_100_2 e_1_2_6_123_1 e_1_2_6_7_2 Evano G. (e_1_2_6_84_2) 2015; 48 e_1_2_6_3_2 e_1_2_6_24_2 e_1_2_6_47_2 e_1_2_6_28_2 e_1_2_6_43_2 e_1_2_6_66_2 e_1_2_6_24_3 e_1_2_6_89_2 e_1_2_6_52_2 e_1_2_6_75_2 e_1_2_6_94_2 e_1_2_6_115_2 e_1_2_6_119_1 e_1_2_6_71_2 e_1_2_6_90_2 e_1_2_6_111_2 e_1_2_6_18_2 e_1_2_6_10_2 e_1_2_6_33_1 e_1_2_6_37_3 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_56_2 e_1_2_6_79_2 e_1_2_6_98_2 e_1_2_6_103_2 e_1_2_6_63_2 e_1_2_6_86_2 e_1_2_6_63_3 e_1_2_6_107_1 e_1_2_6_40_2 e_1_2_6_82_1 e_1_2_6_122_1 e_1_2_6_8_2 e_1_2_6_29_3 e_1_2_6_29_2 e_1_2_6_4_2 e_1_2_6_48_2 e_1_2_6_21_3 e_1_2_6_21_2 e_1_2_6_44_2 e_1_2_6_25_3 e_1_2_6_67_2 e_1_2_6_25_2 e_1_2_6_67_3 Wang, XN (WOS:000331775200026) 2014; 47 Kawada, Y (WOS:000450436100011) 2018; 9 Zhou, AH (WOS:000348147100050) 2015; 6 Shen, WB (WOS:000394996100029) 2017; 56 Davies, PW (WOS:000295383900029) 2011; 50 Ha, HH (WOS:000253410100039) 2008; 18 Xu, Y (WOS:000486836200001) 2019; 58 Sheng, GR (WOS:000424224800031) 2018; 54 Wang, YH (WOS:000354027300003) 2015; 21 Wang, ZS (WOS:000515214000046) 2020; 142 Shu, C (WOS:000359279500017) 2015; 137 Hong, KM (WOS:000467320000075) 2019; 21 Lu, BA (WOS:000295259700028) 2011; 50 Prabagar, B (WOS:000458417700031) 2019; 58 Saundane, AR (WOS:000350365100033) 2015; 24 Li, L (WOS:000461509800030) 2019; 10 Li, CQ (WOS:000288691600041) 2011; 13 Gorin, DJ (WOS:000231227400031) 2005; 127 Zi, WW (WOS:000381438600009) 2016; 45 Mokar, BD (WOS:000432598400014) 2018; 9 Chen, LF (WOS:000438546100010) 2018; 4 Chatzopoulou, E (WOS:000323758900010) 2013; 49 Dutta, S (WOS:000458417700016) 2019; 58 Stoll, AH (WOS:000275085100004) 2010; 132 Dorel, R (WOS:000361254500004) 2015; 115 Wang, YM (WOS:000333235800017) 2014; 47 Van Baelen, G (WOS:000270434000014) 2009; 17 Su, H (WOS:000477946500013) 2019; 6 Shu, C (WOS:000383640600047) 2016; 18 Thornton, AR (WOS:000254933000010) 2008; 130 Deibler, KK (WOS:000402023300011) 2017; 12 Sahani, RL (WOS:000411810600060) 2017; 56 Gronnier, C (WOS:000323363100049) 2013; 15 Li, L (WOS:000402851600036) 2017; 7 Tian, XH (WOS:000508224500001) 2020; 26 Prechter, A (WOS:000335202700037) 2014; 53 Liu, B (WOS:000466620700001) 2019; 170 Xiao, YJ (WOS:000308390000094) 2012; 14 Pawar, SK (WOS:000357984900033) 2015; 21 Mace, N (WOS:000319741100030) 2013; 52 Garzon, M (WOS:000342117600040) 2014; 16 Evano, G (WOS:000366962600001) 2015; 48 Yan, ZY (WOS:000307586900040) 2012; 51 Giri, SS (WOS:000431100800016) 2018; 9 Jia, MQ (WOS:000383371800003) 2016; 55 Stoll, AH (WOS:000285009500014) 2011; 2 Shu, C (WOS:000379455300054) 2016; 18 Parrish, JP (WOS:000186489000032) 2003; 68 Zhang, LM (WOS:000333235800016) 2014; 47 Wu, X (WOS:000501305100010) 2019; 55 Hung, HH (WOS:000323362600017) 2013; 78 Helan, V (WOS:000349832600039) 2015; 6 Obradors, C (WOS:000333235800018) 2014; 47 Wang, LS (WOS:000394736300011) 2017; 19 Li, N (WOS:000382711200008) 2016; 18 Harris, RJ (WOS:000381438600007) 2016; 45 Zhou, B (WOS:000474812400059) 2019; 9 Song, XR (WOS:000390471500002) 2016; 14 Shen, WB (WOS:000416229300034) 2017; 8 Gonzalez, J (WOS:000375880200006) 2016; 358 Wetzel, A (WOS:000293840400028) 2011; 50 Jin, HM (WOS:000385713200016) 2016; 55 Zhang, C (WOS:000386221900016) 2016; 52 Qian, DY (WOS:000348922100006) 2015; 44 Evano, G (WOS:000277131200004) 2010; 49 Zeng, ZY (WOS:000433492900038) 2018; 57 Sahani, RL (WOS:000394997200015) 2017; 56 Hong, FL (WOS:000529156100050) 2020; 142 Cai, J (WOS:000431726900054) 2018; 20 Thornton, AR (WOS:000263576100008) 2009; 131 Tian, XH (WOS:000471212100096) 2019; 21 Tian, XH (WOS:000465644300095) 2019; 21 Jadhav, PD (WOS:000447224100079) 2018; 8 Zeng, Z (WOS:000453346300054) 2018; 57 Matsuoka, J (WOS:000403017000017) 2017; 56 Hashmi, ASK (WOS:000333235800015) 2014; 47 Tian, XH (WOS:000461843900010) 2019; 21 Zhu, XQ (WOS:000502161200001) 2020; 59 Van Baelen, G (WOS:000266695800018) 2009 DeKorver, KA (WOS:000281840400004) 2010; 110 Lourdusamy, E (WOS:000283818600025) 2010; 49 Fensterbank, L (WOS:000333235800022) 2014; 47 Zhu, L (WOS:000347506200009) 2015; 17 Zhou, B (WOS:000476471300042) 2019; 10 Zheng, ZT (WOS:000381438600002) 2016; 45 Tian, XH (WOS:000498470000001) 2020; 59 Tian, XH (WOS:000460318200055) 2019; 58 Li, N (WOS:000350116200015) 2015; 21 Su, H (WOS:000459822800022) 2019; 361 Tokimizu, Y (WOS:000337074300091) 2014; 16 Hong, FL (WOS:000492800500051) 2019; 141 Lonca, GH (WOS:000392424300013) 2017; 53 Aguilar, E (WOS:000466794900028) 2019; 6 Allegue, D (WOS:000459822800015) 2019; 361 Zhou, B (WOS:000397346200044) 2017; 56 Parrish, JP (WOS:000183988300053) 2003; 5 Davies, PW (WOS:000359426800001) 2015; 4 Yeom, HS (WOS:000333235800023) 2014; 47 (000559994700001.1) 2014 Shen, RW (WOS:000449688000032) 2018; 360 Jin, HM (WOS:000368069200063) 2016; 55 Liao, Y (WOS:000414724700016) 2017; 7 |
References_xml | – volume: 142 start-page: 7618 year: 2020 publication-title: J. Am. Chem. Soc. – volume: 55 start-page: 14769 year: 2019 publication-title: Chem. Commun. – volume: 50 123 start-page: 8358 8508 year: 2011 2011 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 45 start-page: 4533 year: 2016 publication-title: Chem. Soc. Rev. – volume: 358 start-page: 1398 year: 2016 publication-title: Adv. Synth. Catal. – volume: 361 start-page: 826 year: 2019 publication-title: Adv. Synth. Catal. – volume: 56 129 start-page: 1026 1046 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 21 start-page: 3328 year: 2019 publication-title: Org. Lett. – volume: 6 start-page: 1928 year: 2015 publication-title: Chem. Sci. – volume: 5 start-page: 2577 year: 2003 publication-title: Org. Lett. – volume: 50 123 start-page: 7354 7492 year: 2011 2011 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 110 start-page: 5064 year: 2010 publication-title: Chem. Rev. – volume: 53 start-page: 736 year: 2017 publication-title: Chem. Commun. – volume: 58 131 start-page: 3589 3627 year: 2019 2019 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 52 125 start-page: 5836 5948 year: 2013 2013 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 58 131 start-page: 16252 16398 year: 2019 2019 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 7 start-page: 4004 year: 2017 publication-title: ACS Catal. – volume: 6 start-page: 1513 year: 2019 publication-title: Org. Chem. Front. – volume: 21 start-page: 4327 year: 2019 publication-title: Org. Lett. – year: 2014 – volume: 16 start-page: 4850 year: 2014 publication-title: Org. Lett. – volume: 56 129 start-page: 605 620 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 47 start-page: 953 year: 2014 publication-title: Acc. Chem. Res. – volume: 47 start-page: 864 year: 2014 publication-title: Acc. Chem. Res. – volume: 49 start-page: 8617 year: 2013 publication-title: Chem. Commun. – volume: 127 start-page: 11260 year: 2005 publication-title: J. Am. Chem. Soc. – volume: 142 start-page: 3636 year: 2020 publication-title: J. Am. Chem. Soc. – volume: 56 129 start-page: 4015 4073 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 68 start-page: 8984 year: 2003 publication-title: J. Org. Chem. – volume: 2 start-page: 112 year: 2011 publication-title: Chem. Sci. – volume: 57 130 start-page: 16549 16787 year: 2018 2018 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 9 start-page: 2991 year: 2018 publication-title: Chem. Sci. – volume: 18 start-page: 4630 year: 2016 publication-title: Org. Lett. – volume: 26 start-page: 3197 year: 2020 publication-title: Chem. Eur. J. – volume: 21 start-page: 2937 year: 2019 publication-title: Org. Lett. – volume: 53 126 start-page: 4959 5059 year: 2014 2014 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 49 122 start-page: 2840 2902 year: 2010 2010 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 52 start-page: 12470 year: 2016 publication-title: Chem. Commun. – volume: 16 start-page: 3138 year: 2014 publication-title: Org. Lett. – volume: 21 start-page: 10843 year: 2015 publication-title: Chem. Eur. J. – volume: 45 start-page: 4567 year: 2016 publication-title: Chem. Soc. Rev. – volume: 21 start-page: 7332 year: 2015 publication-title: Chem. Eur. J. – volume: 115 start-page: 9028 year: 2015 publication-title: Chem. Rev. – volume: 47 start-page: 877 year: 2014 publication-title: Acc. Chem. Res. – volume: 58 131 start-page: 2289 2311 year: 2019 2019 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 130 start-page: 5020 year: 2008 publication-title: J. Am. Chem. Soc. – volume: 21 start-page: 3585 year: 2015 publication-title: Chem. Eur. J. – volume: 14 start-page: 11317 year: 2016 publication-title: Org. Biomol. Chem. – volume: 56 129 start-page: 12736 12910 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 6 start-page: 2404 year: 2019 publication-title: Org. Chem. Front. – volume: 54 start-page: 1529 year: 2018 publication-title: Chem. Commun. – volume: 9 start-page: 4488 year: 2018 publication-title: Chem. Sci. – volume: 47 start-page: 966 year: 2014 publication-title: Acc. Chem. Res. – volume: 132 start-page: 2108 year: 2010 publication-title: J. Am. Chem. Soc. – volume: 360 start-page: 4252 year: 2018 publication-title: Adv. Synth. Catal. – volume: 7 start-page: 7529 year: 2017 publication-title: ACS Catal. – volume: 24 start-page: 1681 year: 2015 publication-title: Med. Chem. Res. – volume: vi start-page: 174 year: 2009 publication-title: ARKIVOC – volume: 58 131 start-page: 2365 2387 year: 2019 2019 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 12 start-page: 1245 year: 2017 publication-title: ACS Chem. Biol. – volume: 15 start-page: 4234 year: 2013 publication-title: Org. Lett. – volume: 78 start-page: 7970 year: 2013 publication-title: J. Org. Chem. – volume: 17 start-page: 7209 year: 2009 publication-title: Bioorg. Med. Chem. – volume: 18 start-page: 3254 year: 2016 publication-title: Org. Lett. – volume: 4 start-page: 1208 year: 2018 publication-title: Chem – volume: 170 start-page: 1 year: 2019 publication-title: Eur. J. Med. Chem. – volume: 137 start-page: 9567 year: 2015 publication-title: J. Am. Chem. Soc. – volume: 141 start-page: 16961 year: 2019 publication-title: J. Am. Chem. Soc. – volume: 10 start-page: 3123 year: 2019 publication-title: Chem. Sci. – volume: 13 start-page: 1738 year: 2011 publication-title: Org. Lett. – volume: 55 128 start-page: 794 804 year: 2016 2016 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 45 start-page: 4448 year: 2016 publication-title: Chem. Soc. Rev. – volume: 47 start-page: 560 year: 2014 publication-title: Acc. Chem. Res. – volume: 18 start-page: 653 year: 2008 publication-title: Bioorg. Med. Chem. Lett. – volume: 4 start-page: 694 year: 2015 publication-title: Asian J. Org. Chem. – volume: 47 start-page: 889 year: 2014 publication-title: Acc. Chem. Res. – volume: 19 start-page: 782 year: 2017 publication-title: Org. Lett. – volume: 131 start-page: 2434 year: 2009 publication-title: J. Am. Chem. Soc. – volume: 6 start-page: 1265 year: 2015 publication-title: Chem. Sci. – volume: 9 start-page: 6393 year: 2019 publication-title: ACS Catal. – volume: 21 start-page: 1598 year: 2019 publication-title: Org. Lett. – volume: 44 start-page: 677 year: 2015 publication-title: Chem. Soc. Rev. – volume: 361 start-page: 758 year: 2019 publication-title: Adv. Synth. Catal. – volume: 14 start-page: 4662 year: 2012 publication-title: Org. Lett. – volume: 51 124 start-page: 8624 8752 year: 2012 2012 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 49 122 start-page: 7963 8135 year: 2010 2010 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 50 123 start-page: 8931 9093 year: 2011 2011 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 57 130 start-page: 6935 7051 year: 2018 2018 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 48 start-page: 59 year: 2015 publication-title: Aldrichimica Acta – volume: 18 start-page: 4178 year: 2016 publication-title: Org. Lett. – volume: 59 132 start-page: 1666 1683 year: 2020 2020 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 59 132 start-page: 471 479 year: 2020 2020 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 56 129 start-page: 7444 7552 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 8 start-page: 1748 year: 2017 publication-title: Nat. Commun. – volume: 20 start-page: 2733 year: 2018 publication-title: Org. Lett. – volume: 55 128 start-page: 9134 9280 year: 2016 2016 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 47 start-page: 902 year: 2014 publication-title: Acc. Chem. Res. – volume: 17 start-page: 30 year: 2015 publication-title: Org. Lett. – volume: 10 start-page: 3234 year: 2019 publication-title: Nat. Commun. – volume: 55 128 start-page: 12688 12880 year: 2016 2016 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 8 start-page: 9697 year: 2018 publication-title: ACS Catal. – volume: 9 start-page: 8416 year: 2018 publication-title: Chem. Sci. – ident: e_1_2_6_37_3 doi: 10.1002/ange.201103563 – ident: e_1_2_6_63_3 doi: 10.1002/ange.201102707 – ident: e_1_2_6_87_2 doi: 10.1002/anie.200905817 – ident: e_1_2_6_68_2 doi: 10.1021/ol5012604 – ident: e_1_2_6_5_2 doi: 10.1039/C5CS00887E – ident: e_1_2_6_54_1 doi: 10.1021/ja053804t – ident: e_1_2_6_51_2 doi: 10.1021/acs.orglett.9b01074 – ident: e_1_2_6_77_2 doi: 10.1002/adsc.201801425 – ident: e_1_2_6_9_2 doi: 10.1039/C4CS00304G – ident: e_1_2_6_45_1 – ident: e_1_2_6_92_3 doi: 10.1002/ange.201908495 – ident: e_1_2_6_40_2 doi: 10.1002/chem.201904869 – ident: e_1_2_6_93_2 doi: 10.1038/s41467-019-11245-2 – ident: e_1_2_6_86_2 doi: 10.1021/cr100003s – ident: e_1_2_6_91_2 doi: 10.1021/jacs.9b09303 – ident: e_1_2_6_11_2 doi: 10.1021/ar4002334 – ident: e_1_2_6_96_2 doi: 10.1021/acscatal.7b01038 – ident: e_1_2_6_25_2 doi: 10.1002/anie.201508309 – ident: e_1_2_6_34_2 doi: 10.1021/ol502346d – ident: e_1_2_6_21_3 doi: 10.1002/ange.201912334 – ident: e_1_2_6_112_2 doi: 10.1021/acschembio.6b01060 – ident: e_1_2_6_80_2 doi: 10.1021/acs.orglett.6b01503 – ident: e_1_2_6_121_2 doi: 10.1021/jo035119f – ident: e_1_2_6_90_2 doi: 10.1021/jacs.9b13975 – ident: e_1_2_6_24_2 doi: 10.1002/anie.201606043 – ident: e_1_2_6_30_3 doi: 10.1002/ange.201610665 – ident: e_1_2_6_88_1 – ident: e_1_2_6_23_3 doi: 10.1002/ange.201802445 – ident: e_1_2_6_76_2 doi: 10.1021/ol503172h – ident: e_1_2_6_7_2 doi: 10.1021/cr500691k – ident: e_1_2_6_50_2 doi: 10.1021/ja908538t – ident: e_1_2_6_65_1 – volume: 48 start-page: 59 year: 2015 ident: e_1_2_6_84_2 publication-title: Aldrichimica Acta – ident: e_1_2_6_59_2 doi: 10.1002/anie.201103014 – ident: e_1_2_6_104_1 – ident: e_1_2_6_10_2 doi: 10.1021/ar4001839 – ident: e_1_2_6_2_2 doi: 10.1016/j.chempr.2018.02.001 – ident: e_1_2_6_21_2 doi: 10.1002/anie.201912334 – ident: e_1_2_6_105_1 doi: 10.1021/acscatal.7b02558 – ident: e_1_2_6_98_2 doi: 10.1039/C7CC09488D – ident: e_1_2_6_56_2 doi: 10.1002/chem.201406456 – ident: e_1_2_6_62_2 doi: 10.1021/ol4019634 – ident: e_1_2_6_57_2 doi: 10.1002/anie.201203678 – ident: e_1_2_6_39_1 – ident: e_1_2_6_67_2 doi: 10.1002/anie.201703279 – ident: e_1_2_6_78_1 – ident: e_1_2_6_61_2 doi: 10.1039/C6CC08397H – ident: e_1_2_6_31_3 doi: 10.1002/ange.201610042 – ident: e_1_2_6_94_2 doi: 10.1039/C9SC00079H – ident: e_1_2_6_100_2 doi: 10.1039/C6CC06864B – ident: e_1_2_6_33_1 – ident: e_1_2_6_6_3 doi: 10.1002/ange.201508119 – ident: e_1_2_6_101_2 doi: 10.1002/anie.201004073 – ident: e_1_2_6_119_1 – ident: e_1_2_6_95_2 doi: 10.1002/anie.201700596 – ident: e_1_2_6_97_1 – ident: e_1_2_6_120_2 doi: 10.1021/ol035000t – ident: e_1_2_6_81_2 doi: 10.1021/jacs.5b06015 – ident: e_1_2_6_87_3 doi: 10.1002/ange.200905817 – ident: e_1_2_6_109_2 doi: 10.1002/anie.201811947 – ident: e_1_2_6_79_2 doi: 10.1021/acs.orglett.6b02267 – ident: e_1_2_6_72_2 doi: 10.1021/acs.orglett.8b00939 – ident: e_1_2_6_74_2 doi: 10.1021/acs.orglett.6b01627 – ident: e_1_2_6_4_2 doi: 10.1039/C6CS00171H – ident: e_1_2_6_28_2 doi: 10.1021/acscatal.8b03011 – ident: e_1_2_6_13_2 doi: 10.1021/ar400188g – ident: e_1_2_6_64_3 doi: 10.1002/ange.201402470 – ident: e_1_2_6_102_2 doi: 10.1002/adsc.201800909 – ident: e_1_2_6_44_2 doi: 10.1021/acs.orglett.9b00140 – ident: e_1_2_6_75_2 doi: 10.1002/chem.201500694 – ident: e_1_2_6_71_2 doi: 10.1039/C9QO00568D – ident: e_1_2_6_99_2 doi: 10.1021/acs.orglett.6b03752 – ident: e_1_2_6_18_2 doi: 10.1039/C6OB01965J – ident: e_1_2_6_114_2 – ident: e_1_2_6_109_3 doi: 10.1002/ange.201811947 – ident: e_1_2_6_48_2 doi: 10.1021/ja7111788 – ident: e_1_2_6_25_3 doi: 10.1002/ange.201508309 – ident: e_1_2_6_110_1 – ident: e_1_2_6_8_2 doi: 10.1002/chem.201406318 – ident: e_1_2_6_17_2 doi: 10.1039/C9QO00243J – ident: e_1_2_6_47_2 doi: 10.1021/ja809078d – ident: e_1_2_6_107_1 – ident: e_1_2_6_123_1 – ident: e_1_2_6_64_2 doi: 10.1002/anie.201402470 – ident: e_1_2_6_38_2 doi: 10.1021/ol2002607 – ident: e_1_2_6_118_2 doi: 10.1002/ange.201912534 – ident: e_1_2_6_35_2 doi: 10.1039/c3cc45410j – ident: e_1_2_6_29_2 doi: 10.1002/anie.201707423 – ident: e_1_2_6_49_2 doi: 10.1039/C0SC00375A – ident: e_1_2_6_24_3 doi: 10.1002/ange.201606043 – ident: e_1_2_6_30_2 doi: 10.1002/anie.201610665 – ident: e_1_2_6_89_2 doi: 10.1021/jacs.0c01918 – ident: e_1_2_6_32_2 doi: 10.1039/C4SC02596B – ident: e_1_2_6_108_3 doi: 10.1002/ange.201813143 – ident: e_1_2_6_111_2 doi: 10.1016/j.ejmech.2019.03.003 – ident: e_1_2_6_14_2 doi: 10.1021/ar400181x – ident: e_1_2_6_63_2 doi: 10.1002/anie.201102707 – ident: e_1_2_6_55_1 – ident: e_1_2_6_113_2 doi: 10.1007/s00044-014-1243-2 – ident: e_1_2_6_69_1 – ident: e_1_2_6_46_2 doi: 10.1002/anie.201301087 – ident: e_1_2_6_52_2 doi: 10.1002/adsc.201801484 – ident: e_1_2_6_92_2 doi: 10.1002/anie.201908495 – ident: e_1_2_6_103_2 doi: 10.1039/C4SC03358B – ident: e_1_2_6_22_2 doi: 10.1002/anie.201810369 – ident: e_1_2_6_53_2 doi: 10.1002/adsc.201600022 – ident: e_1_2_6_83_2 doi: 10.1021/acscatal.9b01851 – ident: e_1_2_6_19_2 doi: 10.1002/ajoc.201500170 – ident: e_1_2_6_116_2 doi: 10.3998/ark.5550190.0010.618 – ident: e_1_2_6_41_2 doi: 10.1002/anie.201812002 – ident: e_1_2_6_106_1 – ident: e_1_2_6_122_1 – ident: e_1_2_6_20_1 – ident: e_1_2_6_95_3 doi: 10.1002/ange.201700596 – ident: e_1_2_6_85_2 doi: 10.1021/ar400193g – ident: e_1_2_6_1_1 – ident: e_1_2_6_115_2 doi: 10.1016/j.bmc.2009.08.057 – ident: e_1_2_6_46_3 doi: 10.1002/ange.201301087 – ident: e_1_2_6_27_2 doi: 10.1039/C8SC00232K – ident: e_1_2_6_58_2 doi: 10.1021/ol302102h – ident: e_1_2_6_82_1 – ident: e_1_2_6_36_2 doi: 10.1021/jo401161h – ident: e_1_2_6_22_3 doi: 10.1002/ange.201810369 – ident: e_1_2_6_60_1 – ident: e_1_2_6_41_3 doi: 10.1002/ange.201812002 – ident: e_1_2_6_3_2 doi: 10.1039/C5CS00929D – ident: e_1_2_6_42_2 doi: 10.1021/acs.orglett.9b01501 – ident: e_1_2_6_37_2 doi: 10.1002/anie.201103563 – ident: e_1_2_6_59_3 doi: 10.1002/ange.201103014 – ident: e_1_2_6_15_2 doi: 10.1021/ar500015k – ident: e_1_2_6_23_2 doi: 10.1002/anie.201802445 – ident: e_1_2_6_70_2 doi: 10.1039/C9CC06652G – ident: e_1_2_6_117_2 doi: 10.1016/j.bmcl.2007.11.064 – ident: e_1_2_6_16_1 – ident: e_1_2_6_43_2 doi: 10.1021/acs.orglett.9b01011 – ident: e_1_2_6_29_3 doi: 10.1002/ange.201707423 – ident: e_1_2_6_57_3 doi: 10.1002/ange.201203678 – ident: e_1_2_6_66_2 doi: 10.1039/C8SC03525C – ident: e_1_2_6_12_2 doi: 10.1021/ar400174p – ident: e_1_2_6_73_2 doi: 10.1038/s41467-017-01853-1 – ident: e_1_2_6_108_2 doi: 10.1002/anie.201813143 – ident: e_1_2_6_118_1 doi: 10.1002/anie.201912534 – ident: e_1_2_6_31_2 doi: 10.1002/anie.201610042 – ident: e_1_2_6_67_3 doi: 10.1002/ange.201703279 – ident: e_1_2_6_6_2 doi: 10.1002/anie.201508119 – ident: e_1_2_6_26_2 doi: 10.1039/C8SC00986D – ident: e_1_2_6_101_3 doi: 10.1002/ange.201004073 – start-page: 174 year: 2009 ident: WOS:000266695800018 article-title: Synthesis of 5-methyl-5H-pyrrolo[2,3-c]quinoline and 4-methyl-4H-pyrrolo[2,3-c]isoquinoline: two new unnatural D-ring stripped isomers of the cryptolepine series publication-title: ARKIVOC doi: 10.3998/ark.5550190.0010.618 – volume: 18 start-page: 3254 year: 2016 ident: WOS:000379455300054 article-title: Gold-Catalyzed Intermolecular Ynamide Amination-Initiated Aza-Nazarov Cyclization: Access to Functionalized 2-Aminopyrroles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b01503 – volume: 6 start-page: 2404 year: 2019 ident: WOS:000477946500013 article-title: Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c9qo00568d – volume: 48 start-page: 59 year: 2015 ident: WOS:000366962600001 article-title: Ynamides: Powerful and Versatile Reagents for Chemical Synthesis publication-title: ALDRICHIMICA ACTA – volume: 54 start-page: 1529 year: 2018 ident: WOS:000424224800031 article-title: A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2 '-oxazolidin]-2-imines publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c7cc09488d – volume: 21 start-page: 2937 year: 2019 ident: WOS:000465644300095 article-title: Gold(III)-Catalyzed Formal [3+2] Annulations of N-Acyl Sulfilimines with Ynamides for the Synthesis of 4-Aminooxazoles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.9b01011 – volume: 8 start-page: ARTN 1748 year: 2017 ident: WOS:000416229300034 article-title: Divergent synthesis of N-heterocycles via controllable cyclization of azido-diynes catalyzed by copper and gold publication-title: NATURE COMMUNICATIONS doi: 10.1038/s41467-017-01853-1 – volume: 115 start-page: 9028 year: 2015 ident: WOS:000361254500004 article-title: Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity publication-title: CHEMICAL REVIEWS doi: 10.1021/cr500691k – volume: 49 start-page: 8617 year: 2013 ident: WOS:000323758900010 article-title: Highly regioselective synthesis of 2,4,5-(hetero) aryl substituted oxazoles by intermolecular [3+2]-cycloaddition of unsymmetrical internal alkynes publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c3cc45410j – volume: 56 start-page: 4015 year: 2017 ident: WOS:000397346200044 article-title: Yttrium-Catalyzed Intramolecular Hydroalkoxylation/Claisen Rearrangement Sequence: Efficient Synthesis of Medium-Sized Lactams publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201700596 – volume: 131 start-page: 2434 year: 2009 ident: WOS:000263576100008 article-title: pi-Nucleophile Traps for Metallonitrene/Alkyne Cascade Reactions: A Versatile Process for the Synthesis of alpha-Aminocyclopropanes and beta-Aminostyrenes publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja809078d – volume: 56 start-page: 605 year: 2017 ident: WOS:000394996100029 article-title: Highly Site Selective Formal [5+2] and [4+2] Annulations of Isoxazoles with Heterosubstituted Alkynes by Platinum Catalysis: Rapid Access to Functionalized 1,3-Oxazepines and 2,5-Dihydropyridines publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201610042 – volume: 2 start-page: 112 year: 2011 ident: WOS:000285009500014 article-title: Rhodium catalyzed allene amidation: a facile entry into 2-amidoallylcations for unusual [3+3] annulation reactions publication-title: CHEMICAL SCIENCE doi: 10.1039/c0sc00375a – volume: 9 start-page: 4488 year: 2018 ident: WOS:000432598400014 article-title: Gold-catalyzed (4+2)-annulations between alpha-alkyl alkenylgold carbenes and benzisoxazoles with reactive alkyl groups publication-title: CHEMICAL SCIENCE doi: 10.1039/c8sc00986d – volume: 18 start-page: 653 year: 2008 ident: WOS:000253410100039 article-title: Novel heterocycle-substituted pyrimidines as inhibitors of NF-kappa B transcription regulation related to TNF-alpha cytokine release publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2007.11.064 – volume: 18 start-page: 4630 year: 2016 ident: WOS:000383640600047 article-title: Synthesis of 2-Aza-1,3-butadienes through Gold-Catalyzed Intermolecular Ynamide Amination/C-H Functionalization publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b02267 – volume: 45 start-page: 4567 year: 2016 ident: WOS:000381438600009 article-title: Recent advances in enantioselective gold catalysis publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c5cs00929d – volume: 58 start-page: 2289 year: 2019 ident: WOS:000458417700016 article-title: Alkyne Versus Ynamide Reactivity: Regioselective Radical Cyclization of Yne-Ynamides publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201811947 – volume: 21 start-page: 1598 year: 2019 ident: WOS:000461843900010 article-title: N-Pyridinyl Sulfilimines as a Source for alpha-Imino Gold Carbenes: Access to 2-Amino-Substituted N-Fused Imidazoles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.9b00140 – volume: 59 start-page: 1666 year: 2020 ident: WOS:000502161200001 article-title: Zinc-Catalyzed Asymmetric Formal [4+3] Annulation of Isoxazoles with Enynol Ethers by 6 pi Electrocyclization: Stereoselective Access to 2H-Azepines publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201912534 – volume: 14 start-page: 11317 year: 2016 ident: WOS:000390471500002 article-title: Recent advances in the tandem reaction of azides with alkynes or alkynols publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c6ob01965j – volume: 56 start-page: 1026 year: 2017 ident: WOS:000394997200015 article-title: Development of Gold-catalyzed [4+1] and [2+2+1]/[4+2] Annulations between Propiolate Derivatives and Isoxazoles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201610665 – volume: 53 start-page: 4959 year: 2014 ident: WOS:000335202700037 article-title: Gold- Catalyzed Synthesis of Functionalized Pyridines by Using 2H-Azirines as Synthetic Equivalents of Alkenyl Nitrenes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201402470 – volume: 52 start-page: 5836 year: 2013 ident: WOS:000319741100030 article-title: Unveiling Latent alpha-Iminocarbene Reactivity for Intermolecular Cascade Reactions through Alkyne Oxidative Amination publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201301087 – volume: 55 start-page: 9134 year: 2016 ident: WOS:000383371800003 article-title: New Approaches to the Synthesis of Metal Carbenes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201508119 – volume: 55 start-page: 14769 year: 2019 ident: WOS:000501305100010 article-title: Gold-catalyzed cyclization of 1-(2 '-azidoaryl) propynols: synthesis of polysubstituted 4-quinolones publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c9cc06652g – volume: 50 start-page: 8931 year: 2011 ident: WOS:000295383900029 article-title: Intermolecular and Selective Synthesis of 2,4,5-Trisubstituted Oxazoles by a Gold-Catalyzed Formal [3+2] Cycloaddition publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201103563 – volume: 5 start-page: 2577 year: 2003 ident: WOS:000183988300053 article-title: Synthesis and X-ray analysis of an unprecedented and stable 2-aza-4,4-spirocyclopropacyclohexadienone publication-title: ORGANIC LETTERS doi: 10.1021/ol035000t – volume: 19 start-page: 782 year: 2017 ident: WOS:000394736300011 article-title: Copper-Catalyzed P-H Insertions of alpha-Imino Carbenes for the Preparation of 3-Phosphinoylindoles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b03752 – volume: 10 start-page: 3123 year: 2019 ident: WOS:000461509800030 article-title: Metal-free alkene carbooxygenation following tandem intramolecular alkoxylation/Claisen rearrangement: stereocontrolled access to bridged [4.2.1] lactones publication-title: CHEMICAL SCIENCE doi: 10.1039/c9sc00079h – volume: 9 start-page: 2991 year: 2018 ident: WOS:000431100800016 article-title: Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles via novel 6 pi-electrocyclizations of 3-azahepta trienyl cations publication-title: CHEMICAL SCIENCE doi: 10.1039/c8sc00232k – volume: 56 start-page: 7444 year: 2017 ident: WOS:000403017000017 article-title: Total Synthesis of Dictyodendrins by the Gold-Catalyzed Cascade Cyclization of Conjugated Diynes with Pyrroles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201703279 – volume: 53 start-page: 736 year: 2017 ident: WOS:000392424300013 article-title: Gold(I)-catalyzed 6-endo-dig azide-yne cyclization: efficient access to 2H-1,3-oxazines publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c6cc08397h – volume: 142 start-page: 7618 year: 2020 ident: WOS:000529156100050 article-title: Copper-Catalyzed Asymmetric Reaction of Alkenyl Diynes with Styrenes by Formal [3+2] Cycloaddition via Cu-Containing AllCarbon 1,3-Dipoles: Access to Chiral Pyrrole-Fused Bridged [2.2.1] Skeletons publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.0c01918 – volume: 44 start-page: 677 year: 2015 ident: WOS:000348922100006 article-title: Gold-catalyzed cyclopropanation reactions using a carbenoid precursor toolbox publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c4cs00304g – volume: 58 start-page: 3589 year: 2019 ident: WOS:000460318200055 article-title: Sulfilimines as Versatile Nitrene Transfer Reagents: Facile Access to Diverse Aza-Heterocycles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201812002 – volume: 47 start-page: 864 year: 2014 ident: WOS:000333235800015 article-title: Dual Gold Catalysis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar500015k – volume: 17 start-page: 30 year: 2015 ident: WOS:000347506200009 article-title: Gold-Catalyzed Intermolecular Nitrene Transfer from 2H-Azirines to Ynamides: A Direct Approach to Polysubstituted Pyrroles publication-title: ORGANIC LETTERS doi: 10.1021/ol503172h – volume: 58 start-page: 2365 year: 2019 ident: WOS:000458417700031 article-title: Umpolung Reactivity of Ynamides: An Unconventional [1,3]-Sulfonyl and [1,5]-Sulfinyl Migration Cascade publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201813143 – volume: 47 start-page: 902 year: 2014 ident: WOS:000333235800018 article-title: Gold-Catalyzed Rearrangements and Beyond publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400174p – volume: 4 start-page: 694 year: 2015 ident: WOS:000359426800001 article-title: Nucleophilic Nitrenoids Through pi-Acid Catalysis: Providing a Common Basis for Rapid Access into Diverse Nitrogen Heterocycles publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ajoc.201500170 – volume: 49 start-page: 2840 year: 2010 ident: WOS:000277131200004 article-title: Ynamides: Versatile Tools in Organic Synthesis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200905817 – volume: 20 start-page: 2733 year: 2018 ident: WOS:000431726900054 article-title: Gold-catalyzed Bicyclization of Diaryl Alkynes: Synthesis of Polycyclic Fused indole and Spirooxindole Derivatives publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.8b00939 – volume: 132 start-page: 2108 year: 2010 ident: WOS:000275085100004 article-title: Rhodium Catalyzed Allene Amination: Diastereoselective Synthesis of Aminocyclopropanes via a 2-Amidoallylcation Intermediate publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja908538t – volume: 127 start-page: 11260 year: 2005 ident: WOS:000231227400031 article-title: Gold(I)-catalyzed intramolecular acetylenic Schmidt reaction publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja053804t – volume: 130 start-page: 5020 year: 2008 ident: WOS:000254933000010 article-title: Catalytic, metallonitrene/alkyne metathesis: A powerful cascade process for the synthesis of nitrogen-containing molecules publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja7111788 – volume: 24 start-page: 1681 year: 2015 ident: WOS:000350365100033 article-title: Synthesis and biological evaluation of novel indolo[2,3-c]isoquinoline derivatives publication-title: MEDICINAL CHEMISTRY RESEARCH doi: 10.1007/s00044-014-1243-2 – volume: 361 start-page: 826 year: 2019 ident: WOS:000459822800022 article-title: Silver-Catalyzed Carbocyclization of Azide-Tethered Alkynes: Expeditious Synthesis of Polysubstituted Quinolines publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201801425 – volume: 55 start-page: 794 year: 2016 ident: WOS:000368069200063 article-title: Gold-Catalyzed C-H Annulation of Anthranils with Alkynes: A Facile, Flexible, and Atom-Economical Synthesis of Unprotected 7-Acylindoles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201508309 – volume: 68 start-page: 8984 year: 2003 ident: WOS:000186489000032 article-title: Synthesis and evaluation of duocarmycin and CC-1065 analogues incorporating the 1,2,9,9a-tetrahydrocyclopropa[c]benz[e]-3-azaindol-4-one (CBA) alkylation subunit publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo035119f – volume: 13 start-page: 1738 year: 2011 ident: WOS:000288691600041 article-title: Gold-Catalyzed Nitrene Transfer to Activated Alkynes: Formation of alpha,beta-Unsaturated Amidines publication-title: ORGANIC LETTERS doi: 10.1021/ol2002607 – volume: 9 start-page: 8416 year: 2018 ident: WOS:000450436100011 article-title: Direct synthesis of aryl-annulated [c]carbazoles by gold(i)-catalysed cascade reaction of azide-diynes and arenes publication-title: CHEMICAL SCIENCE doi: 10.1039/c8sc03525c – volume: 50 start-page: 7354 year: 2011 ident: WOS:000293840400028 article-title: Gold-Catalyzed Transformation of 2-Alkynyl Arylazides: Efficient Access to the Valuable Pseudoindoxyl and Indolyl Frameworks publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201102707 – volume: 49 start-page: 7963 year: 2010 ident: WOS:000283818600025 article-title: Stereoselective Synthesis of alpha-Diazo Oxime Ethers and Their Application in the Synthesis of Highly Substituted Pyrroles through a [3+2] Cycloaddition publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201004073 – volume: 16 start-page: 4850 year: 2014 ident: WOS:000342117600040 article-title: A Direct Route into Fused Imidazo-diazines and Imidazo-pyridines Using Nucleophilic Nitrenoids in a Gold-Catalyzed Formal [3+2]-Dipolar Cycloaddition publication-title: ORGANIC LETTERS doi: 10.1021/ol502346d – volume: 12 start-page: 1245 year: 2017 ident: WOS:000402023300011 article-title: A Chemical Probe Strategy for Interrogating Inhibitor Selectivity Across the MEK Kinase Family publication-title: ACS CHEMICAL BIOLOGY doi: 10.1021/acschembio.6b01060 – volume: 45 start-page: 4533 year: 2016 ident: WOS:000381438600007 article-title: Gold carbenes, gold-stabilized carbocations, and cationic intermediates relevant to gold- catalysed enyne cycloaddition publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c6cs00171h – volume: 57 start-page: 16549 year: 2018 ident: WOS:000453346300054 article-title: Gold(III)-Catalyzed Site-Selective and Divergent Synthesis of 2-Aminopyrroles and Quinoline-Based Polyazaheterocycles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201810369 – volume: 170 start-page: 1 year: 2019 ident: WOS:000466620700001 article-title: Synthesis of novel 7-azaindole derivatives containing pyridin-3-ylmethyl dithiocarbamate moiety as potent PKM2 activators and PKM2 nucleus translocation inhibitors publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1016/j.ejmech.2019.03.003 – volume: 47 start-page: 953 year: 2014 ident: WOS:000333235800022 article-title: Molecular Complexity from Polyunsaturated Substrates: The Gold Catalysis Approach publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar4002334 – volume: 55 start-page: 12688 year: 2016 ident: WOS:000385713200016 article-title: Gold-Catalyzed Synthesis of Quinolines from Propargyl Silyl Ethers and Anthranils through the Umpolung of a Gold Carbene Carbon publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201606043 – volume: 78 start-page: 7970 year: 2013 ident: WOS:000323362600017 article-title: Oxidant-Dependent Chemoselectivity in the Gold-Catalyzed Oxidative Cyclizations of 3,4,6,6-Tetrasubstituted 3,5-Dien-1-ynes publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo401161h – volume: 56 start-page: 12736 year: 2017 ident: WOS:000411810600060 article-title: Gold-Catalyzed [4+2] Annulation/Cyclization Cascades of Benzisoxazoles with Propiolate Derivatives to Access Highly Oxygenated Tetrahydroquinolines publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201707423 – volume: 52 start-page: 12470 year: 2016 ident: WOS:000386221900016 article-title: Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl alpha-iminodiazoacetates publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c6cc06864b – volume: 51 start-page: 8624 year: 2012 ident: WOS:000307586900040 article-title: Gold-Catalyzed One-Step Construction of 2,3-Dihydro-1H-Pyrrolizines with an Electron-Withdrawing group in the 5-position: A Formal Synthesis of 7-Methoxymitosene publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201203678 – volume: 110 start-page: 5064 year: 2010 ident: WOS:000281840400004 article-title: Ynamides: A Modern Functional Group for the New Millennium publication-title: CHEMICAL REVIEWS doi: 10.1021/cr100003s – volume: 141 start-page: 16961 year: 2019 ident: WOS:000492800500051 article-title: Generation of Donor/Donor Copper Carbenes through Copper-Catalyzed Diyne Cyclization: Enantioselective and Divergent Synthesis of Chiral Polycyclic Pyrroles publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.9b09303 – volume: 47 start-page: 877 year: 2014 ident: WOS:000333235800016 article-title: A Non-Diazo Approach to alpha-Oxo Gold Carbenes via Gold-Catalyzed Alkyne Oxidation publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400181x – volume: 47 start-page: 560 year: 2014 ident: WOS:000331775200026 article-title: Ynamides in Ring Forming Transformations publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400193g – volume: 361 start-page: 758 year: 2019 ident: WOS:000459822800015 article-title: Regiodivergent Control in the Gold(I) Catalyzed Synthesis of 7-Pyrazolylindoles from 1-Propargyl-1H-benzotriazoles and Ynamides through alpha-Imino Gold(I) Carbene Complexes publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201801484 – volume: 21 start-page: 10843 year: 2015 ident: WOS:000357984900033 article-title: Diversity in Gold-Catalyzed Formal Cycloadditions of Ynamides with Azidoalkenes or 2H-Azirines: [3+2] versus [4+3] Cycloadditions publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201500694 – volume: 47 start-page: 966 year: 2014 ident: WOS:000333235800023 article-title: Catalytic Access to alpha-Oxo Gold Carbenes by N-O Bond Oxidants publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar4001839 – volume: 45 start-page: 4448 year: 2016 ident: WOS:000381438600002 article-title: Au-Catalysed oxidative cyclisation publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c5cs00887e – volume: 10 start-page: ARTN 3234 year: 2019 ident: WOS:000476471300042 article-title: Stereoselective synthesis of medium lactams enabled by metal-free hydroalkoxylation/stereospecific [1,3]-rearrangement publication-title: NATURE COMMUNICATIONS doi: 10.1038/s41467-019-11245-2 – volume: 21 start-page: 3585 year: 2015 ident: WOS:000350116200015 article-title: Gold-Catalyzed Multiple Cascade Reaction of 2-Alkynylphenylazides with Propargyl Alcohols publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201406456 – volume: 4 start-page: 1208 year: 2018 ident: WOS:000438546100010 article-title: Transition-Metal-Catalyzed Intramolecular Nucleophilic Addition of Carbonyl Groups to Alkynes publication-title: CHEM doi: 10.1016/j.chempr.2018.02.001 – volume: 6 start-page: 1513 year: 2019 ident: WOS:000466794900028 article-title: Gold-catalyzed heterocyclic syntheses through alpha-imino gold carbene complexes as intermediates Dedicated to Professor Dr Julius Rebek, Jr. on the occasion of his 75th birthday. publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c9qo00243j – volume: 18 start-page: 4178 year: 2016 ident: WOS:000382711200008 article-title: Gold-Catalyzed Direct Assembly of Aryl-Annulated Carbazoles from 2-Alkynyl Arylazides and Alkynes publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b01627 – volume: 14 start-page: 4662 year: 2012 ident: WOS:000308390000094 article-title: Synthesis of Bicyclic Imidazoles via [2+3] Cycloaddition between Nitriles and Regioselectively Generated alpha-Imino Gold Carbene Intermediates publication-title: ORGANIC LETTERS doi: 10.1021/ol302102h – year: 2014 ident: 000559994700001.1 publication-title: PCT Int. Appl. WO – volume: 6 start-page: 1265 year: 2015 ident: WOS:000348147100050 article-title: Atom-economic generation of gold carbenes: gold-catalyzed formal [3+2] cycloaddition between ynamides and isoxazoles publication-title: CHEMICAL SCIENCE doi: 10.1039/c4sc02596b – volume: 9 start-page: 6393 year: 2019 ident: WOS:000474812400059 article-title: Reversal of Regioselectivity in Ynamide Chemistry publication-title: ACS CATALYSIS doi: 10.1021/acscatal.9b01851 – volume: 21 start-page: 3328 year: 2019 ident: WOS:000467320000075 article-title: Rhodium-Catalyzed Nitrene/Alkyne Metathesis: An Enantioselective Process for the Synthesis of N-Heterocycles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.9b01074 – volume: 7 start-page: 4004 year: 2017 ident: WOS:000402851600036 article-title: Reversal of Regioselectivity in Catalytic Arene-Ynamide Cyclization: Direct Synthesis of Valuable Azepino[4,5-b]indoles and beta-Carbolines and DFT Calculations publication-title: ACS CATALYSIS doi: 10.1021/acscatal.7b01038 – volume: 21 start-page: 4327 year: 2019 ident: WOS:000471212100096 article-title: Synthesis of 2-Aminoindoles through Gold-Catalyzed C-H Annulations of Sulfilimines with N-Arylynamides publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.9b01501 – volume: 360 start-page: 4252 year: 2018 ident: WOS:000449688000032 article-title: Copper(II) Acetate-Catalyzed Synthesis of Phosphorylated Pyridines via Denitrogenative C-P Coupling between Pyridotriazoles and P(O)H Compounds publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201800909 – volume: 26 start-page: 3197 year: 2020 ident: WOS:000508224500001 article-title: alpha-Imino Gold Carbene Intermediates from Readily Accessible Sulfilimines: Intermolecular Access to Structural Diversity publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201904869 – volume: 7 start-page: 7529 year: 2017 ident: WOS:000414724700016 article-title: Rhodium-Catalyzed Azide-Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions publication-title: ACS CATALYSIS doi: 10.1021/acscatal.7b02558 – volume: 358 start-page: 1398 year: 2016 ident: WOS:000375880200006 article-title: One-Pot and Regioselective Gold-Catalyzed Synthesis of 2-Imidazolyl-1-pyrazolylbenzenes from 1-Propargyl-1H-benzotriazoles, Alkynes and Nitriles through -Imino Gold(I) Carbene Complexes publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600022 – volume: 57 start-page: 6935 year: 2018 ident: WOS:000433492900038 article-title: Gold-Catalyzed Regiospecific C-H Annulation of o-Ethynylbiaryls with Anthranils: pi-Extension by Ring-Expansion En Route to N-Doped PAHs publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201802445 – volume: 142 start-page: 3636 year: 2020 ident: WOS:000515214000046 article-title: Ynamide Smiles Rearrangement Triggered by Visible-Light-Mediated Regioselective Ketyl-Ynamide Coupling: Rapid Access to Functionalized Indoles and Isoquinolines publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.9b13975 – volume: 15 start-page: 4234 year: 2013 ident: WOS:000323363100049 article-title: Au-Catalyzed Formation of Functionalized Quinolines from 2-Alkynyl Arylazide Derivatives publication-title: ORGANIC LETTERS doi: 10.1021/ol4019634 – volume: 8 start-page: 9697 year: 2018 ident: WOS:000447224100079 article-title: Gold-Catalyzed [5+2]- and [5+1]-Annulations between Ynamides and 1,2-Benzisoxazoles with Ligand-Controlled Chemoselectivity publication-title: ACS CATALYSIS doi: 10.1021/acscatal.8b03011 – volume: 6 start-page: 1928 year: 2015 ident: WOS:000349832600039 article-title: Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: efficient synthesis of indolizines publication-title: CHEMICAL SCIENCE doi: 10.1039/c4sc03358b – volume: 21 start-page: 7332 year: 2015 ident: WOS:000354027300003 article-title: Gold Carbene or Carbenoid: Is There a Difference? publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201406318 – volume: 50 start-page: 8358 year: 2011 ident: WOS:000295259700028 article-title: Umpolung Reactivity of Indole through Gold Catalysis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201103014 – volume: 17 start-page: 7209 year: 2009 ident: WOS:000270434000014 article-title: Structure-activity relationship of antiparasitic and cytotoxic indoloquinoline alkaloids, and their tricyclic and bicyclic analogues publication-title: BIOORGANIC & MEDICINAL CHEMISTRY doi: 10.1016/j.bmc.2009.08.057 – volume: 16 start-page: 3138 year: 2014 ident: WOS:000337074300091 article-title: Gold-Catalyzed Cascade Cyclization of (Azido)ynamides: An Efficient Strategy for the Construction of Indoloquinolines publication-title: ORGANIC LETTERS doi: 10.1021/ol5012604 – volume: 59 start-page: 471 year: 2020 ident: WOS:000498470000001 article-title: Acyl Migration versus Epoxidation in Gold Catalysis: Facile, Switchable, and Atom-Economic Synthesis of Acylindoles and Quinoline Derivatives publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201912334 – volume: 47 start-page: 889 year: 2014 ident: WOS:000333235800017 article-title: Development of Catalysts and Ligands for Enantioselective Gold Catalysis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400188g – volume: 58 start-page: 16252 year: 2019 ident: WOS:000486836200001 article-title: Organocatalytic Enantioselective Conia-Ene-Type Carbocyclization of Ynamide Cyclohexanones: Regiodivergent Synthesis of Morphans and Normorphans publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201908495 – volume: 137 start-page: 9567 year: 2015 ident: WOS:000359279500017 article-title: Generation of alpha-Imin Gold Carbenes through Gold-Catalyzed Intermolecular Reaction of Azides with Ynamides publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b06015 |
SSID | ssj0028806 |
Score | 2.580713 |
Snippet | Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first... Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via alpha-imino copper carbene intermediates is reported, representing the first... Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via α-imino copper carbene intermediates is reported, representing the first... |
Source | Web of Science |
SourceID | proquest webofscience crossref wiley |
SourceType | Aggregation Database Enrichment Source Index Database Publisher |
StartPage | 17984 |
SubjectTerms | Alkynes asymmetric catalysis Asymmetry Carbenes Catalysts Chemistry Chemistry, Multidisciplinary Copper cyclizations Divergence Enantiomers heterocycles Intermediates Physical Sciences Science & Technology Substrates |
Title | Copper‐Catalyzed Azide–Ynamide Cyclization to Generate α‐Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N‐Heterocycles |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202007206 http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000559994700001 https://www.proquest.com/docview/2446718397 https://www.proquest.com/docview/2420155546 |
Volume | 59 |
WOS | 000559994700001 |
WOSCitedRecordID | wos000559994700001 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NjtMwELbQXuDCPyKwICOtxCm7aRzbDbcqdNVFokKIlZZT5J-xVFGSqk0P7WkfYaU98hS8CA-xT4Inf7tFQiC4JfFfbM_En52Zbwg5cHqY2sSK0BqJRzdREqooSfwuBbhNeWqFQgfn91MxOU3enfGzG178DT9Ef-CGmlF_r1HBlV4dXZOGoge239_hWVtcc26jwRaioo89f1TshbNxL2IsxCj0HWtjFB_tFt9dla6h5s5itItf6wXo-B5R3as3didfDteVPjTbX1gd_6dv98ndFp3SUSNOD8gtKB6S21kXFO4R-ZaViwUsr84vMjz32WzB0tF2ZuHq_PIzxra3QLONmbfenbQqaUNsXQH98d0XO_k6K0ra1EIztdT4rX1D36J5CHp5UVVYOkbrnFm5qmP0-BQ6qsM6Ym0fyvnGYAOGTn11E7TmKfEBrB6T0-Pxp2wStvEdQsN4JEJt44H2gNSBkU7rgWbKQCqRgcakwwSYTYUDxqWSThrmkaMysRgy8LAIjI7YE7JXlAU8JVQZ5yLFhUr8LttaDKDupPZgTMfghDMBCbv5zU1Lfo4xOOZ5Q9sc5zjkeT_kAXnd5180tB-_zbnfiUveqv8q95hJSMSeMiCv-mQ_Vfg3RhVQrjFPjHiVJ76Kg5ti1jeIeJp7AO81CKF4QAZ_ky1ru4ecBlVA4lrO_tCJfDQ9Gfd3z_6l0HNyB69rO0e-T_aq5RpeeLxW6Ze1Tv4Eg149yA |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lb9NAEB6VcigX3ohAgUUq4uTWWb9iJA6RkyqhbYRQK5WT2ZeliNSuEkcoOfUnIHHkV_SPcOAn9Jcw41cJEgIh9cDNj_U63t3Z-WYy8w3AViI7oXa1b2kVkOvGdi1huy5aKcbToRdqX1CC88HIHxy5b4694zU4r3NhSn6IxuFGklHs1yTg5JDeuWQNpRRsNPDI2cZtv4qr3DOLT2i1zV4PezjFLzjf7R9GA6sqLGApx0MLWmreloiEEqOCRMq2dIQyYUDUJyrsuMbRoZ8YxwtEkATKQcgiFPc7jkF9bJS0Hez3GlynMuJE19971zBWcRSHMqHJcSyqe1_zRNp8Z_X3rurBS3C7ov5WEXOh8nZvwfd6sMpIl4_b81xuq-UvPJL_1WjehpsVAGfdUmLuwJpJ78JGVNe9uwdfo-z01Ewvzj5H5NpaLI1m3eVYm4uzL-9TcYJHLFqoSZXAyvKMldzduWHfzvGx4ck4zVjZC4vEVJI6ecV6FAFDiWxMpJr1KQBpnM2KMkR4h3WLypXU29tsslD0AsVG2N2AApYyumBm9-HoSsbmAaynWWoeAhMqSWzh-cLlgas11YhPAol4U3KT-IlqgVUvqFhV_O5UZmQSl8zUPKYpjpspbsHLpv1pyWzy25ab9fqMqx1uFiMs9AOC10ELnje3caroDyeRmmxObThBcs_FLrZ-XtfNC8lk8NBGwU2CrI0WtP-mWVR9HtE25C3gxcL-w0fE3dGw35w9-peHnsHG4PBgP94fjvYeww26XoR1epuwnk_n5gnC01w-LTYEBh-uWmZ-AF6tnJQ |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lb9NAEB6VIgEX3giXAotUxMmts37FSBwiJ1FCIaoQlcrJ7FOKmtpR4gglp_4EJI78CfgjSPyF_hJ2_CpBQiCkHrj5sR7Huzs732xmvgHY0bwdSU8GthQhbt04ns0czzNeivJl5EcyYJjg_HoUDA69l0f-0QZ8qXNhSn6IZsMNNaNYr1HBp1LvnZOGYga28e9wr406QRVWua-WH4zTNn8x7JoRfkppv_c2HthVXQFbuL5xoLmkLW6AkFYi1Jy3uMuEikJkPhFR21OujAKtXD9koQ6FaxALEzRou8qYYyW44xq5l-CyFzgRFovovmkIq6jRhjKfyXVtLHtf00Q6dG_9966bwXNsu2b91gFzYfH6N-B73VdloMvx7iLnu2L1C43k_9SZN-F6Bb9Jp9SXW7Ch0ttwNa6r3t2Bz3E2narZ2enHGDe2lislSWc1lurs9NO7lJ2YIxIvxaRKXyV5Rkrm7lyRb1_NY8OTcZqRUgqJ2YyjMXlOuhj_gmlshKWS9DD8aJzNiyJE5g7pFHUrUdpBNlkKfIEgIyNugOFKGV5Q87tweCF9cw820yxV94EwobXD_IB5NPSkxArxOuQGbXKqdKCFBXY9nxJRsbtjkZFJUvJS0wSHOGmG2IJnTftpyWvy25bb9fRMqvVtnhhQGIQIrkMLnjS3zVDh300sVdkC21AE5L5nROz8PK2bF6LD4BsPxSwR6GtY0PqbZnH1eUjakFtAi3n9h49IOqNhrznb-peHHsOVg24_eTUc7T-Aa3i5iOn0t2Ezny3UQ4NNc_6oWA4IvL9olfkB6c6bQw |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Copper%E2%80%90Catalyzed+Azide%E2%80%93Ynamide+Cyclization+to+Generate+%CE%B1%E2%80%90Imino+Copper+Carbenes%3A+Divergent+and+Enantioselective+Access+to+Polycyclic+N%E2%80%90Heterocycles&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Liu%2C+Xin&rft.au=Wang%2C+Ze%E2%80%90Shu&rft.au=Zhai%2C+Tong%E2%80%90Yi&rft.au=Luo%2C+Chen&rft.date=2020-10-05&rft.issn=1433-7851&rft.eissn=1521-3773&rft.volume=59&rft.issue=41&rft.spage=17984&rft.epage=17990&rft_id=info:doi/10.1002%2Fanie.202007206&rft.externalDBID=n%2Fa&rft.externalDocID=10_1002_anie_202007206 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon |