Visible Light‐Induced [3+2] Annulation Reaction of Alkenes with Vinyl Azides: Direct Synthesis of Functionalized Pyrroles
Comprehensive Summary A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts. Broad substrate scope and high functional group tolerance were demonstrated by more than 50 examples. The reaction prov...
Saved in:
| Published in | Chinese journal of chemistry Vol. 42; no. 2; pp. 151 - 156 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY‐VCH Verlag GmbH & Co. KGaA
15.01.2024
Wiley Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Comprehensive Summary
A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts. Broad substrate scope and high functional group tolerance were demonstrated by more than 50 examples. The reaction provides a novel and efficient method for the synthesis of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives.
A visible‐light‐induced catalytic [3+2] annulation of alkenes with vinyl azides was developed in the presence of organic dye photocatalysts. The reaction provides a novel and efficient strategy for the construction of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives. |
|---|---|
| AbstractList | Comprehensive SummaryA photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts. Broad substrate scope and high functional group tolerance were demonstrated by more than 50 examples. The reaction provides a novel and efficient method for the synthesis of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives. A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts. Broad substrate scope and high functional group tolerance were demonstrated by more than 50 examples. The reaction provides a novel and efficient method for the synthesis of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives. Comprehensive Summary A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts. Broad substrate scope and high functional group tolerance were demonstrated by more than 50 examples. The reaction provides a novel and efficient method for the synthesis of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives. A visible‐light‐induced catalytic [3+2] annulation of alkenes with vinyl azides was developed in the presence of organic dye photocatalysts. The reaction provides a novel and efficient strategy for the construction of polyfunctionalized pyrroles under very mild metal‐free conditions without other additives. |
| Author | Wang, Xin‐Yu Zhao, Yu‐Long Yang, Ming Wang, Jie |
| Author_xml | – sequence: 1 givenname: Ming surname: Yang fullname: Yang, Ming organization: Northeast Normal University – sequence: 2 givenname: Xin‐Yu surname: Wang fullname: Wang, Xin‐Yu organization: Northeast Normal University – sequence: 3 givenname: Jie surname: Wang fullname: Wang, Jie organization: Northeast Normal University – sequence: 4 givenname: Yu‐Long surname: Zhao fullname: Zhao, Yu‐Long email: zhaoyl351@nenu.edu.cn organization: Northeast Normal University |
| BookMark | eNqNkclqHDEQQEVwIF5y9VmQo-mxll5zGzrxxoCDnZiAMY1aXZ3RRJEcSY1p--JPyDfmS6xZsCEQEkGhOrxXVVTtoC1jDSC0T8mEEsIO5cLKCSOME5JW5Su0TXOaJgXJs62YE0KTnKRf36Ad7xeRLwqWb6OHK-VVqwHP1Ld5-P3469R0g4QOX_MDdoOnxgxaBGUNvgAhV4nt8VR_BwMe36kwx1fKjBpP71UH_j3-oBzIgC9HE-bglV_iR4NZqUKr-1j60-ic1eD30OteaA9vN_8u-nL08XN9kszOj0_r6SyRnBZlkkHWtsCBSCq6GEKmHLo2TwXLRNqVRV-QjqayZTlvu77PZEbbXorlHiBnnO-id-u6t87-HMCHZmEHF6fxDasIrUrOMhKpck3dQWt7LxUYCc2tUz-EG5u4PlIxnlUliY_WKqy2UtvBhKge_L8a6cmals5676B_Jilplpdslpdsni8ZhfQPQW7aByeU_rtWbaZSGsZ_NGnqs_P6xX0Ch-m2Cw |
| CitedBy_id | crossref_primary_10_1039_D4CC00777H crossref_primary_10_1039_D4CC03484H crossref_primary_10_1039_D4GC04495A crossref_primary_10_1021_acs_orglett_4c03998 crossref_primary_10_1002_cjoc_202300683 crossref_primary_10_1039_D3QO02055J |
| Cites_doi | 10.1021/acs.accounts.9b00142 10.1126/science.aac9895 10.3390/catal10091054 10.1021/acs.joc.2c02267 10.1039/C9CS00523D 10.1021/acs.orglett.8b03147 10.1039/C8NP00051D 10.1002/cjoc.202200732 10.1021/acs.accounts.0c00417 10.1039/C7QO00790F 10.2174/13852728113179990040 10.1021/acs.joc.8b02459 10.1038/s41467-017-02148-1 10.1039/C7CS00339K 10.1039/C3CS60015G 10.1002/cjoc.202100050 10.1021/acs.joc.8b00878 10.1002/ajoc.202200254 10.1002/asia.201901068 10.1038/s41467-017-01853-1 10.1021/acs.chemrev.0c00348 10.1021/acscatal.7b02818 10.1021/acs.orglett.2c00283 10.1016/j.ccr.2016.11.011 10.1021/jacs.5b06015 10.1021/acs.accounts.6b00254 10.1039/D1QO01506K 10.1021/acs.orglett.2c04050 10.1021/acs.chemrev.1c00247 10.1002/anie.202007206 10.1039/D0QO00994F 10.1021/acs.chemrev.6b00018 10.1039/C7CS00017K 10.1016/j.cclet.2022.05.002 10.1016/j.chempr.2019.01.010 10.1039/C4RA15710A 10.1039/C9CS00311H 10.1021/acs.jmedchem.9b00717 10.1002/anie.201400602 10.1021/acs.accounts.6b00263 10.1002/adsc.202000562 10.1039/C6NP00070C 10.1016/j.cclet.2018.05.025 10.1039/C5OB00099H 10.1039/C5CS00659G 10.1021/acs.orglett.6b01059 10.1021/cr078199m 10.1002/anie.202216923 10.1021/acs.accounts.7b00275 10.1021/acs.orglett.0c02835 10.1039/C8CS00790J 10.1002/slct.201700952 10.1021/acs.orglett.9b01416 10.1021/acs.orglett.9b02731 10.1002/anie.201308820 10.1039/c7qo00790f 10.1039/c3cs60015g 10.1039/c7cs00017k 10.1039/c8cs00790j 10.1039/c7cs00339k 10.1039/c5cs00659g 10.1039/c4ra15710a 10.1039/c5ob00099h 10.1039/d0qo00994f 10.1039/d1qo01506k 10.1039/c8np00051d 10.1039/c9cs00311h 10.1039/c6np00070c 10.1039/c9cs00523d |
| ContentType | Journal Article |
| Copyright | 2023 SIOC, CAS, Shanghai, & WILEY‐VCH GmbH 2024 SIOC, CAS, Shanghai, & WILEY‐VCH GmbH |
| Copyright_xml | – notice: 2023 SIOC, CAS, Shanghai, & WILEY‐VCH GmbH – notice: 2024 SIOC, CAS, Shanghai, & WILEY‐VCH GmbH |
| DBID | AAYXX CITATION 17B 1KM 1KN BLEPL DTL EGQ |
| DOI | 10.1002/cjoc.202300498 |
| DatabaseName | CrossRef Web of Knowledge Index Chemicus Current Chemical Reactions Web of Science Core Collection Science Citation Index Expanded Web of Science Primary (SCIE, SSCI & AHCI) |
| DatabaseTitle | CrossRef Web of Science |
| DatabaseTitleList | 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 | 1614-7065 |
| EndPage | 156 |
| ExternalDocumentID | 001092359800001 10_1002_cjoc_202300498 CJOC202300498 |
| Genre | researchArticle |
| GrantInformation_xml | – fundername: We are grateful for the financial support of this research by the National Natural Sciences Foundation of China (21871044 and 21472017).; National Natural Science Foundation of China (NSFC) grantid: 21871044; 21472017 – fundername: National Natural Sciences Foundation of China; National Natural Science Foundation of China (NSFC) |
| GroupedDBID | .3N .GA 05W 0R~ 10A 1L6 1OB 1OC 29B 33P 3SF 3WU 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 5GY 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM AAESR AAEVG AAHQN AAMMB AAMNL AANLZ AAONW AAXRX AAYCA AAZKR ABCQN ABCUV ABDBF ABEML ABIJN ABJNI ABPVW ACAHQ ACCZN ACGFS ACIWK ACPOU ACSCC ACUHS ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN AEFGJ AEIGN AEIMD AENEX AEUYR AEYWJ AFBPY AFFPM AFGKR AFRAH AFWVQ AGHNM AGXDD AGYGG AHBTC AIDQK AIDYY AITYG AIURR AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMYDB ATUGU AUFTA AZBYB AZVAB BAFTC BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BY8 CCEZO CDRFL CHBEP CS3 CW9 D-E D-F DCZOG DPXWK DR2 DRFUL DRSTM EBS F00 F01 F04 G-S G.N GODZA H.T H.X HGLYW HZ~ IX1 J0M JPC LATKE LAW LC2 LC3 LEEKS LITHE LOXES LP6 LP7 LUTES LYRES MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ O66 O9- OIG P2W P4D Q.N Q11 QB0 QRW R.K RNS ROL RX1 RYL SUPJJ W8V W99 WBFHL WBKPD WIH WIK WOHZO WQJ WXSBR WYISQ XG1 XV2 ZZTAW ~IA ~WT AAHHS AAYXX ACCFJ ADZOD AEEZP AEQDE AIWBW AJBDE CITATION FA0 17B 1KM 1KN BLEPL DTL GROUPED_WOS_WEB_OF_SCIENCE |
| ID | FETCH-LOGICAL-c3178-5e5bbe3e0c1adc1aac43edb64a25a4d87f70d14cb263bdff5c51bfca3004e6233 |
| IEDL.DBID | DR2 |
| ISICitedReferencesCount | 9 |
| ISICitedReferencesURI | https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=001092359800001 |
| ISSN | 1001-604X |
| IngestDate | Fri Jul 25 11:11:39 EDT 2025 Fri Aug 29 16:06:38 EDT 2025 Wed Jul 09 18:39:40 EDT 2025 Tue Jul 01 03:35:33 EDT 2025 Thu Apr 24 23:04:43 EDT 2025 Sun Jul 06 04:45:14 EDT 2025 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 2 |
| Keywords | CATALYSIS Vinyl azides Alkenes Radical reactions Photocatalysis Pyrroles Annulation |
| Language | English |
| LinkModel | DirectLink |
| LogoURL | https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg |
| MergedId | FETCHMERGED-LOGICAL-c3178-5e5bbe3e0c1adc1aac43edb64a25a4d87f70d14cb263bdff5c51bfca3004e6233 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
| PQID | 2901983250 |
| PQPubID | 986331 |
| PageCount | 6 |
| ParticipantIDs | proquest_journals_2901983250 webofscience_primary_001092359800001CitationCount webofscience_primary_001092359800001 wiley_primary_10_1002_cjoc_202300498_CJOC202300498 crossref_primary_10_1002_cjoc_202300498 crossref_citationtrail_10_1002_cjoc_202300498 |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | 15 January 2024 |
| PublicationDateYYYYMMDD | 2024-01-15 |
| PublicationDate_xml | – month: 01 year: 2024 text: 15 January 2024 day: 15 |
| PublicationDecade | 2020 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim – name: WEINHEIM – name: Shanghai |
| PublicationTitle | Chinese journal of chemistry |
| PublicationTitleAbbrev | CHINESE J CHEM |
| PublicationYear | 2024 |
| Publisher | WILEY‐VCH Verlag GmbH & Co. KGaA Wiley Wiley Subscription Services, Inc |
| Publisher_xml | – name: WILEY‐VCH Verlag GmbH & Co. KGaA – name: Wiley – name: Wiley Subscription Services, Inc |
| References | 2017 2018; 50 29 2022 2017 2015 2020 2021 2015 2020 2017 2023 2023 2021; 11 46 13 53 121 137 59 8 62 41 39 2017; 8 2023 2020 2022 2020 2022; 25 7 9 22 87 2022 2016 2020 2019 2019 2018; 24 18 362 14 21 83 2013 2014 2023; 17 43 34 2019 2018 2017 2017 2020 2018; 84 20 2 7 362 5 2019 2019; 52 62 2016 2016 2019 2016 2020 2019 2019 2020; 33 49 5 49 10 48 21 49 2015; 349 2019 2008; 36 108 2015 2017; 5 333 2022 2022 2017 2016 2016; 51 122 46 45 116 2014; 53 e_1_2_5_9_4 e_1_2_5_11_5 e_1_2_5_15_1 e_1_2_5_7_5 e_1_2_5_9_3 e_1_2_5_11_4 e_1_2_5_7_4 e_1_2_5_9_2 e_1_2_5_15_3 e_1_2_5_7_3 e_1_2_5_9_1 e_1_2_5_11_6 e_1_2_5_15_2 e_1_2_5_7_2 e_1_2_5_11_1 e_1_2_5_7_1 e_1_2_5_5_2 e_1_2_5_11_3 e_1_2_5_13_1 e_1_2_5_5_1 e_1_2_5_11_2 e_1_2_5_3_2 e_1_2_5_3_1 e_1_2_5_15_5 e_1_2_5_15_4 e_1_2_5_9_6 e_1_2_5_9_5 e_1_2_5_8_5 e_1_2_5_10_6 e_1_2_5_8_4 e_1_2_5_10_5 e_1_2_5_14_1 e_1_2_5_8_3 e_1_2_5_10_8 e_1_2_5_10_10 e_1_2_5_8_2 e_1_2_5_10_7 e_1_2_5_10_11 e_1_2_5_16_1 e_1_2_5_6_3 e_1_2_5_8_1 e_1_2_5_10_2 e_1_2_5_6_2 e_1_2_5_10_1 e_1_2_5_6_1 e_1_2_5_10_4 e_1_2_5_4_2 e_1_2_5_10_3 e_1_2_5_12_1 e_1_2_5_4_1 e_1_2_5_2_2 e_1_2_5_2_1 e_1_2_5_10_9 e_1_2_5_8_8 e_1_2_5_8_7 e_1_2_5_8_6 Liang, YX (WOS:000577160700046) 2020; 22 Huang, XQ (WOS:000418567200012) 2017; 8 Hu, B (WOS:000351597700001) 2015; 13 Chen, JR (WOS:000384038600033) 2016; 49 Fu, JK (WOS:000417020300007) 2017; 46 Shu, C (WOS:000359279500017) 2015; 137 Hu, XQ (WOS:000582051400001) 2020; 10 Krzeszewski, M (WOS:000411548800029) 2017; 50 Nicholls, TP (WOS:000387064800001) 2016; 33 Xie, J (WOS:000408580300002) 2017; 46 Liu, X (WOS:000559994700001) 2020; 59 Xuan, J (WOS:000337041600028) 2014; 53 Borra, S (WOS:000546635700001) 2020; 362 Estévez, V (WOS:000337131200017) 2014; 43 Shen, WB (WOS:000416229300034) 2017; 8 Festa, AA (WOS:000480621900002) 2019; 48 Mao, LL (WOS:000422863300013) 2018; 5 Borra, S (WOS:000456632800055) 2019; 84 Calvete, MJF (WOS:000392771000006) 2017; 333 Sahoo, AK (WOS:000773353800008) 2022; 24 Lei, T (WOS:000376476300039) 2016; 18 Kundu, T (WOS:000475543300023) 2019; 62 Bhardwaj, V (WOS:000349435000038) 2015; 5 Lei, WL (WOS:000451101500053) 2018; 20 Pitre, SP (WOS:000765830800006) 2022; 122 Hong, FL (WOS:000572833000027) 2020; 53 Fan, H (WOS:000252257800007) 2008; 108 Lang, XJ (WOS:000378260000001) 2016; 45 Farney, EP (WOS:000330983300027) 2014; 53 Liu, Y (WOS:000489200100021) 2019; 21 Wood, JM (WOS:000459332300001) 2019; 36 Yang, M (WOS:000729459800001) 2022; 9 Romero, NA (WOS:000361357700046) 2015; 349 Karki, BS (WOS:000493021400001) 2019; 14 Hatai, J (WOS:000472683000021) 2019; 52 Borkotoky, L (WOS:000815025000001) 2022; 11 Shi, ZW (WOS:000901797800001) 2023; 34 Joshi, SD (WOS:000326079200008) 2013; 17 Cheng, YZ (WOS:000760929500001) 2022; 51 Liang, YX (WOS:000904570400001) 2023; 25 Liu, X (WOS:000920585100001) 2023; 62 Reddy, NNK (WOS:000442451500049) 2018; 83 Xuan, J (WOS:000533976700002) 2020; 49 Xu, LH (WOS:000953255000001) 2023; 41 Börjesson, M (WOS:000458660100002) 2019; 5 Ye, LW (WOS:000679894900014) 2021; 121 Wu, CL (WOS:000438004700018) 2018; 29 Yang, M (WOS:000582936400019) 2020; 7 Morris, SA (WOS:000384038600037) 2016; 49 Adiyala, PR (WOS:000411188600063) 2017; 2 Xu, XC (WOS:000893110200001) 2022; 87 Skubi, KL (WOS:000383410100010) 2016; 116 Lei, WL (WOS:000414724700067) 2017; 7 Liang, Q (WOS:000658286100001) 2021; 39 Cai, BG (WOS:000471212100077) 2019; 21 |
| References_xml | – volume: 51 122 46 45 116 start-page: 2145 1717 5193 3026 10035 year: 2022 2022 2017 2016 2016 end-page: 2170 1751 5203 3038 10074 article-title: Visible‐light induced dearomatization reactions Strategic Use of Visible‐Light Photoredox Catalysis in Natural Product Synthesis The recent achievements of redox‐neutral radical C‐C cross‐coupling enabled by visible‐light Cooperative photoredox catalysis Dual Catalysis Strategies in Photochemical Synthesis publication-title: Chem. Soc. Rev. Chem. Rev. Chem. Soc. Rev. Chem. Soc. Rev. Chem. Rev. – volume: 11 46 13 53 121 137 59 8 62 41 39 start-page: 7208 3844 2003 9039 9567 17984 1748 1191 1948 year: 2022 2017 2015 2020 2021 2015 2020 2017 2023 2023 2021 end-page: 7228 3855 2019 9112 9570 17990 1197 1952 article-title: Recent Advances on ‐Azidoketones and Esters in the Synthesis of ‐Heterocycles alpha‐Substituted vinyl azides: an emerging functionalized alkene Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis Transition Metal‐Catalyzed Tandem Reactions of Ynamides for Divergent ‐Heterocycle Synthesis Nitrene Transfer and Carbene Transfer in Gold Catalysis Generation of α‐Imino Gold Carbenes through Gold‐Catalyzed Intermolecular Reaction of Azides with Ynamides Copper‐Catalyzed Azide–Ynamide Cyclization to Generate α‐Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N‐Heterocycles Divergent synthesis of N‐heterocycles via controllable cyclization of azido‐diynes catalyzed by copper and gold Copper‐Catalyzed Enantioselective Doyle–Kirmse Reaction of Azide‐Ynamides via α‐Imino Copper Carbenes Radical Decarboxylative Cyanomethylation of Aliphatic Carboxylic Acids and Uronic Acids via Vinyl Azide Cascade Fragmentation Synthesis of Phenanthridine and Quinoxaline Derivatives via Copper‐Catalyzed Radical Cyanoalkylation of Cyclobutanone Oxime Esters and Vinyl Azides publication-title: Asian J. Org. Chem. Chem. Soc. Rev. Org. Biomol. Chem. Acc. Chem. Res. Chem. Rev. J. Am. Chem. Soc. Angew. Chem. Int. Ed. Nat. Commun. Angew. Chem. Int. Ed. Chin. J. Chem. Chin. J. Chem. – volume: 84 20 2 7 362 5 start-page: 1042 7220 8158 7941 3364 232 year: 2019 2018 2017 2017 2020 2018 end-page: 1052 7224 8161 7945 3368 236 article-title: Access to 2,3‐Fused Pyrroles via Visible Light Driven Coupling of alpha‐Azidochalcones with 1/2‐Naphthols, or 2‐Hydroxy‐1,4‐Naphthoquinone Eosin Y‐ and Copper‐Catalyzed Dark Reaction to Construct Ene‐gamma‐Lactams Visible Light Driven Coupling of 2‐aminopyridines and ‐Keto Vinyl Azides for the Synthesis of Imidazo[1, 2‐ ]pyridines and Their Cytotoxicity Visible‐Light‐Driven Synthesis of 4‐Alkyl/Aryl‐2‐ Aminothiazoles Promoted by Generated Copper Photocatalyst Photocatalyst‐Free Visible‐Light Enabled Synthesis of Substituted Pyrroles from ‐Keto Vinyl Azides Visible‐light‐induced sulfonylation/cyclization of vinyl azides: one‐pot construction of 6‐(sulfonylmethyl)phenanthridines publication-title: J. Org. Chem. Org. Lett. ChemistrySelect ACS Catal. Adv. Synth. Catal. Org. Chem. Front. – volume: 25 7 9 22 87 start-page: 200 3493 407 7640 16604 year: 2023 2020 2022 2020 2022 end-page: 204 3498 412 7644 16616 article-title: Lewis Acid Mediated Conjugate Addition of Isocyanides to beta‐Hydroxy‐alpha‐diazo Carbonyls: Synthesis of beta‐Carboxamido‐alpha‐diazo Carbonyl Compounds Rhodium/copper‐cocatalyzed coupling‐cyclization of ‐alkenyl arylisocyanides with vinyl azides: one‐pot synthesis of ‐carbolines Rhodium‐catalyzed coupling‐cyclization reaction of isocyanides and 2‐azidophenyloxyacrylates: synthesis of ‐(3‐substituted benzo[ ]oxazol‐2(3 )‐ylidene)amines and dihydrobenzo[ ]oxazoles Silver‐Catalyzed Cascade Cyclization Reaction of Isocyanides with Sulfoxonium Ylides: Synthesis of 3‐Aminofurans and 4‐Aminoquinolines Visible Light‐Induced Coupling Cyclization Reaction of alpha‐Diazosulfonium Triflates with alpha‐Oxocarboxylic Acids or Alkynes publication-title: Org. Lett. Org. Chem. Front. Org. Chem. Front. Org. Lett. J. Org. Chem. – volume: 53 start-page: 793 year: 2014 end-page: 797 article-title: Visible‐light sensitization of vinyl azides by transition‐metal photocatalysis publication-title: Angew. Chem. Int. Ed. – volume: 53 start-page: 5653 year: 2014 end-page: 5656 article-title: Visible‐light‐induced formal [3+2] cycloaddition for pyrrole synthesis under metal‐free conditions publication-title: Angew. Chem. Int. Ed. – volume: 33 49 5 49 10 48 21 49 start-page: 1248 1911 254 1957 1054 4401 4234 2546 year: 2016 2016 2019 2016 2020 2019 2019 2020 end-page: 1254 1923 256 1968 4423 4238 2556 article-title: Applications of visible light photoredox catalysis to the synthesis of natural products and related compounds Exploration of Visible‐Light Photocatalysis in Heterocycle Synthesis and Functionalization: Reaction Design and Beyond N‐Containing Heterocycles on Demand by Merging Ni Catalysis and Photoredox PCET The Prowess of Photogenerated Amine Radical Cations in Cascade Reactions: From Carbocycles to Heterocycles Radical Carbonylative Synthesis of Heterocycles by Visible Light Photoredox Catalysis Visible light‐mediated chemistry of indoles and related heterocycles [3 + 2]‐Cycloaddition of 2 ‐Azirines with Nitrosoarenes: Visible‐Light‐Promoted Synthesis of 2,5‐Dihydro‐1,2,4‐ oxadiazoles Visible light‐promoted ring‐opening functionalization of three‐membered carbo‐ and heterocycles publication-title: Nat. Prod. Rep. Acc. Chem. Res. Chem Acc. Chem. Res. Catalysts Chem. Soc. Rev. Org. Lett. Chem. Soc. Rev. – volume: 17 43 34 start-page: 2279 4633 year: 2013 2014 2023 end-page: 2304 4657 article-title: Pyrrole: Chemical Synthesis, Microwave Assisted Synthesis, Reactions and Applications: A Review Recent advances in the synthesis of pyrroles by multicomponent reactions Au‐catalyzed neighboring hydroxymethyl group directed cycloaddition of alkyne with diazadienes: Synthesis of polysubstituted pyrroles publication-title: Curr. Org. Chem. Chem. Soc. Rev. Chin. Chem. Lett. – volume: 36 108 start-page: 289 264 year: 2019 2008 end-page: 306 287 article-title: 2‐Formylpyrrole natural products: origin, structural diversity, bioactivity and synthesis Lamellarins and Related Pyrrole‐Derived Alkaloids from Marine Organisms publication-title: Nat. Prod. Rep. Chem. Rev. – volume: 50 29 start-page: 2334 1105 year: 2017 2018 end-page: 2345 1112 article-title: The Tetraarylpyrrolo[3,2‐ ]pyrroles‐From Serendipitous Discovery to Promising Heterocyclic Optoelectronic Materials Programmable pyrrole‐imidazole polyamides: A potent tool for DNA targeting publication-title: Acc. Chem. Res. Chin. Chem. Lett. – volume: 8 start-page: 2245 year: 2017 article-title: Catalytic asymmetric synthesis of a nitrogen heterocycle through stereocontrolled direct photoreaction from electronically excited state publication-title: Nat. Commun. – volume: 5 333 start-page: 15233 82 year: 2015 2017 end-page: 15266 107 article-title: Pyrrole: a resourceful small molecule in key medicinal hetero‐aromatics Metal coordinated pyrrole‐based macrocycles as contrast agents for magnetic resonance imaging technologies: Synthesis and applications publication-title: RSC Adv. Coord. Chem. Rev. – volume: 349 start-page: 1326 year: 2015 end-page: 1330 article-title: Site‐selective arene C‐H amination via photoredox catalysis publication-title: Science – volume: 24 18 362 14 21 83 start-page: 1918 2479 3364 4793 7782 9412 year: 2022 2016 2020 2019 2019 2018 end-page: 1923 2482 3368 4797 7786 9421 article-title: Visible‐Light‐Mediated Synthesis of Thio‐Functionalized Pyrroles Visible Light Initiated Hantzsch Synthesis of 2,5‐Diaryl‐Substituted Pyrroles at Ambient Conditions Photocatalyst‐Free Visible‐Light Enabled Synthesis of Substituted Pyrroles from α‐Keto Vinyl Azides Visible Light‐Induced, Metal‐Free Denitrative [3+2] Cycloaddition for Trisubstituted Pyrrole Synthesis Visible‐Light‐Driven Synthesis of 1,3,4‐Trisubstituted Pyrroles from Aryl Azides Visible‐Light‐Induced C (sp )‐H Functionalization of Tosylhydrazones: Synthesis of Polysubstituted Pyrroles under Metal‐Free Conditions publication-title: Org. Lett. Org. Lett. Adv. Synth. Catal. Chem. Asian. J. Org. Lett. J. Org. Chem. – volume: 52 62 start-page: 1709 6315 year: 2019 2019 end-page: 1720 6329 article-title: Diverse Properties of Guanidiniocarbonyl Pyrrole‐Based Molecules: Artificial Analogues of Arginine Synthesis and Biological Assessment of Pyrrolobenzoxazine Scaffold as a Potent Antioxidant publication-title: Acc. Chem. Res. J. Med. Chem. – ident: e_1_2_5_3_1 doi: 10.1021/acs.accounts.9b00142 – ident: e_1_2_5_16_1 doi: 10.1126/science.aac9895 – ident: e_1_2_5_8_5 doi: 10.3390/catal10091054 – ident: e_1_2_5_15_5 doi: 10.1021/acs.joc.2c02267 – ident: e_1_2_5_8_8 doi: 10.1039/C9CS00523D – ident: e_1_2_5_11_2 doi: 10.1021/acs.orglett.8b03147 – ident: e_1_2_5_2_1 doi: 10.1039/C8NP00051D – ident: e_1_2_5_10_10 doi: 10.1002/cjoc.202200732 – ident: e_1_2_5_10_4 doi: 10.1021/acs.accounts.0c00417 – ident: e_1_2_5_11_6 doi: 10.1039/C7QO00790F – ident: e_1_2_5_6_1 doi: 10.2174/13852728113179990040 – ident: e_1_2_5_11_1 doi: 10.1021/acs.joc.8b02459 – ident: e_1_2_5_14_1 doi: 10.1038/s41467-017-02148-1 – ident: e_1_2_5_7_3 doi: 10.1039/C7CS00339K – ident: e_1_2_5_6_2 doi: 10.1039/C3CS60015G – ident: e_1_2_5_10_11 doi: 10.1002/cjoc.202100050 – ident: e_1_2_5_9_6 doi: 10.1021/acs.joc.8b00878 – ident: e_1_2_5_10_1 doi: 10.1002/ajoc.202200254 – ident: e_1_2_5_9_4 doi: 10.1002/asia.201901068 – ident: e_1_2_5_10_8 doi: 10.1038/s41467-017-01853-1 – ident: e_1_2_5_10_5 doi: 10.1021/acs.chemrev.0c00348 – ident: e_1_2_5_11_4 doi: 10.1021/acscatal.7b02818 – ident: e_1_2_5_9_1 doi: 10.1021/acs.orglett.2c00283 – ident: e_1_2_5_5_2 doi: 10.1016/j.ccr.2016.11.011 – ident: e_1_2_5_10_6 doi: 10.1021/jacs.5b06015 – ident: e_1_2_5_8_2 doi: 10.1021/acs.accounts.6b00254 – ident: e_1_2_5_15_3 doi: 10.1039/D1QO01506K – ident: e_1_2_5_15_1 doi: 10.1021/acs.orglett.2c04050 – ident: e_1_2_5_7_2 doi: 10.1021/acs.chemrev.1c00247 – ident: e_1_2_5_10_7 doi: 10.1002/anie.202007206 – ident: e_1_2_5_15_2 doi: 10.1039/D0QO00994F – ident: e_1_2_5_7_5 doi: 10.1021/acs.chemrev.6b00018 – ident: e_1_2_5_10_2 doi: 10.1039/C7CS00017K – ident: e_1_2_5_6_3 doi: 10.1016/j.cclet.2022.05.002 – ident: e_1_2_5_8_3 doi: 10.1016/j.chempr.2019.01.010 – ident: e_1_2_5_5_1 doi: 10.1039/C4RA15710A – ident: e_1_2_5_7_1 doi: 10.1039/C9CS00311H – ident: e_1_2_5_3_2 doi: 10.1021/acs.jmedchem.9b00717 – ident: e_1_2_5_13_1 doi: 10.1002/anie.201400602 – ident: e_1_2_5_8_4 doi: 10.1021/acs.accounts.6b00263 – ident: e_1_2_5_11_5 doi: 10.1002/adsc.202000562 – ident: e_1_2_5_8_1 doi: 10.1039/C6NP00070C – ident: e_1_2_5_4_2 doi: 10.1016/j.cclet.2018.05.025 – ident: e_1_2_5_10_3 doi: 10.1039/C5OB00099H – ident: e_1_2_5_7_4 doi: 10.1039/C5CS00659G – ident: e_1_2_5_9_2 doi: 10.1021/acs.orglett.6b01059 – ident: e_1_2_5_2_2 doi: 10.1021/cr078199m – ident: e_1_2_5_10_9 doi: 10.1002/anie.202216923 – ident: e_1_2_5_4_1 doi: 10.1021/acs.accounts.7b00275 – ident: e_1_2_5_15_4 doi: 10.1021/acs.orglett.0c02835 – ident: e_1_2_5_8_6 doi: 10.1039/C8CS00790J – ident: e_1_2_5_9_3 doi: 10.1002/adsc.202000562 – ident: e_1_2_5_11_3 doi: 10.1002/slct.201700952 – ident: e_1_2_5_8_7 doi: 10.1021/acs.orglett.9b01416 – ident: e_1_2_5_9_5 doi: 10.1021/acs.orglett.9b02731 – ident: e_1_2_5_12_1 doi: 10.1002/anie.201308820 – volume: 14 start-page: 4793 year: 2019 ident: WOS:000493021400001 article-title: Visible Light-Induced, Metal-Free Denitrative [3+2] Cycloaddition for Trisubstituted Pyrrole Synthesis publication-title: CHEMISTRY-AN ASIAN JOURNAL doi: 10.1002/asia.201901068 – volume: 29 start-page: 1105 year: 2018 ident: WOS:000438004700018 article-title: Programmable pyrrole-imidazole polyamides: A potent tool for DNA targeting publication-title: CHINESE CHEMICAL LETTERS doi: 10.1016/j.cclet.2018.05.025 – volume: 53 start-page: 2003 year: 2020 ident: WOS:000572833000027 article-title: Transition Metal-Catalyzed Tandem Reactions of Ynamides for Divergent N-Heterocycle Synthesis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.0c00417 – volume: 108 start-page: 264 year: 2008 ident: WOS:000252257800007 article-title: Lamellarins and related pyrrole-derived alkaloids from marine organisms publication-title: CHEMICAL REVIEWS doi: 10.1021/cr078199m – volume: 49 start-page: 1957 year: 2016 ident: WOS:000384038600037 article-title: The Prowess of Photogenerated Amine Radical Cations in Cascade Reactions: From Carbocycles to Heterocycles publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.6b00263 – 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: 8 start-page: ARTN 2245 year: 2017 ident: WOS:000418567200012 article-title: Catalytic asymmetric synthesis of a nitrogen heterocycle through stereocontrolled direct photoreaction from electronically excited state publication-title: NATURE COMMUNICATIONS doi: 10.1038/s41467-017-02148-1 – volume: 84 start-page: 1042 year: 2019 ident: WOS:000456632800055 article-title: Access to 2,3-Fused Pyrroles via Visible Light Driven Coupling of α-Azidochalcones with 1/2-Naphthols, or 2-Hydroxy-1,4-Naphthoquinone publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.8b02459 – volume: 34 start-page: ARTN 107488 year: 2023 ident: WOS:000901797800001 article-title: Au-catalyzed neighboring hydroxymethyl group directed cycloaddition of alkyne with diazadienes: Synthesis of polysubstituted pyrroles publication-title: CHINESE CHEMICAL LETTERS doi: 10.1016/j.cclet.2022.05.002 – volume: 5 start-page: 232 year: 2018 ident: WOS:000422863300013 article-title: Visible-light-induced sulfonylation/cyclization of vinyl azides: one-pot construction of 6-(sulfonylmethyl)phenanthridines publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c7qo00790f – volume: 17 start-page: 2279 year: 2013 ident: WOS:000326079200008 article-title: Pyrrole: Chemical Synthesis, Microwave Assisted Synthesis, Reactions and Applications: A Review publication-title: CURRENT ORGANIC CHEMISTRY – volume: 137 start-page: 9567 year: 2015 ident: WOS:000359279500017 article-title: Generation of α-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 – volume: 116 start-page: 10035 year: 2016 ident: WOS:000383410100010 article-title: Dual Catalysis Strategies in Photochemical Synthesis publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.6b00018 – volume: 41 start-page: 1191 year: 2023 ident: WOS:000953255000001 article-title: Radical Decarboxylative Cyanomethylation of Aliphatic Carboxylic Acids and Uronic Acids via Vinyl Azide Cascade Fragmentation publication-title: CHINESE JOURNAL OF CHEMISTRY doi: 10.1002/cjoc.202200732 – volume: 59 start-page: 17984 year: 2020 ident: WOS:000559994700001 article-title: Copper-Catalyzed Azide-Ynamide Cyclization to Generate α-Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N-Heterocycles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202007206 – volume: 7 start-page: 7941 year: 2017 ident: WOS:000414724700067 article-title: Visible-Light-Driven Synthesis of 4-Alkyl/Aryl-2-Aminothiazoles Promoted by In Situ Generated Copper Photocatalyst publication-title: ACS CATALYSIS doi: 10.1021/acscatal.7b02818 – volume: 10 start-page: ARTN 1054 year: 2020 ident: WOS:000582051400001 article-title: Radical Carbonylative Synthesis of Heterocycles by Visible Light Photoredox Catalysis publication-title: CATALYSTS doi: 10.3390/catal10091054 – volume: 87 start-page: 16604 year: 2022 ident: WOS:000893110200001 article-title: Visible Light-Induced Coupling Cyclization Reaction of α-Diazosulfonium Triflates with α-Oxocarboxylic Acids or Alkynes publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.2c02267 – volume: 43 start-page: 4633 year: 2014 ident: WOS:000337131200017 article-title: Recent advances in the synthesis of pyrroles by multicomponent reactions publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c3cs60015g – volume: 22 start-page: 7640 year: 2020 ident: WOS:000577160700046 article-title: Silver-Catalyzed Cascade Cyclization Reaction of Isocyanides with Sulfoxonium Ylides: Synthesis of 3-Aminofurans and 4-Aminoquinolines publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.0c02835 – volume: 50 start-page: 2334 year: 2017 ident: WOS:000411548800029 article-title: The Tetraarylpyrrolo[3,2-b]pyrroles-From Serendipitous Discovery to Promising Heterocyclic Optoelectronic Materials publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.7b00275 – volume: 333 start-page: 82 year: 2017 ident: WOS:000392771000006 article-title: Metal coordinated pyrrole-based macrocycles as contrast agents for magnetic resonance imaging technologies: Synthesis and applications publication-title: COORDINATION CHEMISTRY REVIEWS doi: 10.1016/j.ccr.2016.11.011 – volume: 62 year: 2023 ident: WOS:000920585100001 article-title: Copper-Catalyzed Enantioselective Doyle-Kirmse Reaction of Azide-Ynamides via α-Imino Copper Carbenes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202216923 – volume: 46 start-page: 7208 year: 2017 ident: WOS:000417020300007 article-title: α-Substituted vinyl azides: an emerging functionalized alkene publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c7cs00017k – volume: 48 start-page: 4401 year: 2019 ident: WOS:000480621900002 article-title: Visible light-mediated chemistry of indoles and related heterocycles publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c8cs00790j – volume: 2 start-page: 8158 year: 2017 ident: WOS:000411188600063 article-title: Visible Light Driven Coupling of 2-aminopyridines and α-Keto Vinyl Azides for the Synthesis of Imidazo[1,2-a]pyridines and Their Cytotoxicity publication-title: CHEMISTRYSELECT doi: 10.1002/slct.201700952 – volume: 46 start-page: 5193 year: 2017 ident: WOS:000408580300002 article-title: The recent achievements of redox-neutral radical C-C cross-coupling enabled by visible-light publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c7cs00339k – volume: 121 start-page: 9039 year: 2021 ident: WOS:000679894900014 article-title: Nitrene Transfer and Carbene Transfer in Gold Catalysis publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.0c00348 – volume: 45 start-page: 3026 year: 2016 ident: WOS:000378260000001 article-title: Cooperative photoredox catalysis publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c5cs00659g – volume: 49 start-page: 1911 year: 2016 ident: WOS:000384038600033 article-title: Exploration of Visible-Light Photocatalysis in Heterocycle Synthesis and Functionalization: Reaction Design and Beyond publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.6b00254 – volume: 62 start-page: 6315 year: 2019 ident: WOS:000475543300023 article-title: Synthesis and Biological Assessment of Pyrrolobenzoxazine Scaffold as a Potent Antioxidant publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/acs.jmedchem.9b00717 – volume: 349 start-page: 1326 year: 2015 ident: WOS:000361357700046 article-title: Site-selective arene C-H amination via photoredox catalysis publication-title: SCIENCE doi: 10.1126/science.aac9895 – volume: 5 start-page: 15233 year: 2015 ident: WOS:000349435000038 article-title: Pyrrole: a resourceful small molecule in key medicinal hetero-aromatics publication-title: RSC ADVANCES doi: 10.1039/c4ra15710a – volume: 13 start-page: 3844 year: 2015 ident: WOS:000351597700001 article-title: Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c5ob00099h – volume: 25 start-page: 200 year: 2023 ident: WOS:000904570400001 article-title: Lewis Acid Mediated Conjugate Addition of Isocyanides to β-Hydroxy-a-diazo Carbonyls: Synthesis of β-Carboxamido-a-diazo Carbonyl Compounds publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.2c04050 – volume: 7 start-page: 3493 year: 2020 ident: WOS:000582936400019 article-title: Rhodium/copper-cocatalyzed coupling-cyclization of o-alkenyl arylisocyanides with vinyl azides: one-pot synthesis of α-carbolines publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/d0qo00994f – volume: 52 start-page: 1709 year: 2019 ident: WOS:000472683000021 article-title: Diverse Properties of Guanidiniocarbonyl Pyrrole-Based Molecules: Artificial Analogues of Arginine publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.9b00142 – volume: 39 start-page: 1948 year: 2021 ident: WOS:000658286100001 article-title: Synthesis of Phenanthridine and Quinoxaline Derivatives via Copper-Catalyzed Radical Cyanoalkylation of Cyclobutanone Oxime Esters and Vinyl Azides publication-title: CHINESE JOURNAL OF CHEMISTRY doi: 10.1002/cjoc.202100050 – volume: 9 start-page: 407 year: 2022 ident: WOS:000729459800001 article-title: Rhodium-catalyzed coupling-cyclization reaction of isocyanides and 2-azidophenyloxyacrylates: synthesis of N-(3-substituted benzo[d]oxazol-2(3H)-ylidene)amines and dihydrobenzo[d]oxazoles publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/d1qo01506k – volume: 362 start-page: 3364 year: 2020 ident: WOS:000546635700001 article-title: Photocatalyst-Free Visible-Light Enabled Synthesis of Substituted Pyrroles from α-Keto Vinyl Azides publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.202000562 – volume: 5 start-page: 254 year: 2019 ident: WOS:000458660100002 article-title: N-Containing Heterocycles on Demand by Merging Ni Catalysis and Photoredox PCET publication-title: CHEM doi: 10.1016/j.chempr.2019.01.010 – volume: 24 start-page: 1918 year: 2022 ident: WOS:000773353800008 article-title: Visible-Light-Mediated Synthesis of Thio-Functionalized Pyrroles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.2c00283 – volume: 36 start-page: 289 year: 2019 ident: WOS:000459332300001 article-title: 2-Formylpyrrole natural products: origin, structural diversity, bioactivity and synthesis publication-title: NATURAL PRODUCT REPORTS doi: 10.1039/c8np00051d – volume: 11 start-page: ARTN e202200254 year: 2022 ident: WOS:000815025000001 article-title: Recent Advances on α-Azidoketones and Esters in the Synthesis of N-Heterocycles publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ajoc.202200254 – volume: 21 start-page: 4234 year: 2019 ident: WOS:000471212100077 article-title: [3+2]-Cycloaddition of 2H-Azirines with Nitrosoarenes: Visible-Light-Promoted Synthesis of 2,5-Dihydro-1,2,4-oxadiazoles publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.9b01416 – volume: 53 start-page: 5653 year: 2014 ident: WOS:000337041600028 article-title: Visible-Light-Induced Formal [3+2] Cycloaddition for Pyrrole Synthesis under Metal-Free Conditions publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201400602 – volume: 21 start-page: 7782 year: 2019 ident: WOS:000489200100021 article-title: Visible-Light-Driven Synthesis of 1,3,4-Trisubstituted Pyrroles from Aryl Azides publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.9b02731 – volume: 51 start-page: 2145 year: 2022 ident: WOS:000760929500001 article-title: Visible-light induced dearomatization reactions publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c9cs00311h – volume: 122 start-page: 1717 year: 2022 ident: WOS:000765830800006 article-title: Strategic Use of Visible-Light Photoredox Catalysis in Natural Product Synthesis publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.1c00247 – volume: 33 start-page: 1248 year: 2016 ident: WOS:000387064800001 article-title: Applications of visible light photoredox catalysis to the synthesis of natural products and related compounds publication-title: NATURAL PRODUCT REPORTS doi: 10.1039/c6np00070c – volume: 53 start-page: 793 year: 2014 ident: WOS:000330983300027 article-title: Visible-Light Sensitization of Vinyl Azides by Transition-Metal Photocatalysis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201308820 – volume: 49 start-page: 2546 year: 2020 ident: WOS:000533976700002 article-title: Visible light-promoted ring-opening functionalization of three-membered carbo- and heterocycles publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c9cs00523d – volume: 20 start-page: 7220 year: 2018 ident: WOS:000451101500053 article-title: Eosin Y- and Copper -Catalyzed Dark Reaction To Construct Ene-γ-Lactams publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.8b03147 – volume: 83 start-page: 9412 year: 2018 ident: WOS:000442451500049 article-title: Visible-Light-Induced C (sp3)-H Functionalization of Tosylhydrazones: Synthesis of Polysubstituted Pyrroles under Metal-Free Conditions publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.8b00878 – volume: 18 start-page: 2479 year: 2016 ident: WOS:000376476300039 article-title: Visible Light Initiated Hantzsch Synthesis of 2,5-Diaryl-Substituted Pyrroles at Ambient Conditions publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b01059 |
| SSID | ssj0027726 |
| Score | 2.3662436 |
| Snippet | Comprehensive Summary
A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of... A photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic dye photocatalysts.... Comprehensive SummaryA photocatalytic [3+2] annulation of alkenes with vinyl azides was developed under irradiation by visible light in the presence of organic... |
| Source | Web of Science |
| SourceID | proquest webofscience crossref wiley |
| SourceType | Aggregation Database Enrichment Source Index Database Publisher |
| StartPage | 151 |
| SubjectTerms | Additives Alkenes Annulation Chemical reactions Chemical synthesis Chemistry Chemistry, Multidisciplinary Functional groups Irradiation Organic chemistry Photocatalysis Physical Sciences Pyrroles Radical reactions Science & Technology Substrates Vinyl azides |
| Title | Visible Light‐Induced [3+2] Annulation Reaction of Alkenes with Vinyl Azides: Direct Synthesis of Functionalized Pyrroles |
| URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcjoc.202300498 http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=001092359800001 https://www.proquest.com/docview/2901983250 |
| Volume | 42 |
| WOS | 001092359800001 |
| WOSCitedRecordID | wos001092359800001 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1La9wwEB5KLu2lbfqgbpOiQ6CHosSWLT96C6ZLCH2RNmGhFKMnuFm8Jd4cdnvpT-hvzC-JxrK92UJpaQ8GGyRbkmc0n6SZbwD2jEhlnllBw7yQNMliS6XlguYqtM4C6lgwDE5--y49Ok2Op3x6I4rf80OMG26oGd18jQouZHuwJg1VX-dIQciQMqrAaF902EJUdMLWK66sy7eGPEM0DZPpwNoYsoPN6ptWaQ01N4zRJn7tDNDkHoih6d7v5Hz_ciH31eoXVsf_6dt9uNujU3LoxWkbbpnmAdwuh6RwD-H7We10aGbIG1zUX_34iak_lNHkc_ySfSHI1u-d68iJ8SETZG7J4ewcp1SCm77krG6W7hOrWpv2FfFTLvm4bBwSbesWi0-crfVblPXKvfrD8gJ9INtHcDp5_ak8on3-BqocKskpN1xKE5tQRUK7S6gkNlqmiWBcJNqJSBbqKFGSpbHU1nLFI2mVwF4bB8vix7DVzBvzBEjKpOJOiGyWCYcpsoIzG8ZMFYlbEencBECH_1epntwcc2zMKk_LzCoc0moc0gBejOW_eVqP35bcGcSh6tW7rfDwuXBzIQ8D2LspIuPLuiNHhvSI3flJANHfFCv7piMfwSIA1snIHxpYlcfvy_Hp6b9UegZ33D16I9GI78DW4uLS7DqstZDPO326Bs_vIjo |
| linkProvider | Wiley-Blackwell |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB5BOZQLb9RAAR8qcUBuEyfOg1sVsVrKtqDSVpUQivyUQldZ1GwPu1z4CfxGfgmevJZFQiA45JBonNjOPO3xNwA7RsQyTaygfppJGiWhpdJyQVPlW2cBdSgYHk4-PIrHp9HBOe-zCfEsTIsPMSy4oWQ0-hoFHBek91aooerTDDEIGWJGZel1uIFlvZuo6pitYq6kqbiGSEM09qPzHrfRZ3vr7dft0srZXDNH6x5sY4JGt0H2nW8zTy52r-ZyVy1_wXX8r9HdgVudg0r2W466C9dMdQ82874u3H34clY6MZoaMsG4_vvXb1j9QxlNPoQv2EeCgP1tfh05Nu2pCTKzZH96gVqV4LovOSurhfvEstSmfklarUveLyrnjNZljeQjZ27bVcpy6V79bnGJaZD1AzgdvTrJx7Qr4UCVc0xSyg2X0oTGV4HQ7hIqCo2WcSQYF5F2XJL4OoiUZHEotbVc8UBaJXDUxnlm4UPYqGaV2QISM6m44yObJMK5FUnGmfVDprLIBUU6NR7Q_gcWqsM3xzIb06JFZmYFTmkxTKkHzwf6zy2yx28pt3t-KDoJrwvcf86cOuS-Bzs_88jwsmbXkSFCYrOF4kHwN2R513WEJJh7wBom-UMHi_zgbT7cPfqXRs9gc3xyOCkmr4_ePIab7jkmJ9GAb8PG_PLKPHGu11w-bYTrB-H3JlU |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB5BkYALb0SggA-VOCC3iRPnwa0KrEoppSq0WglVkZ9S6CpbNdvDLhd-Ar-RX4Inr-0iIRAcckjkd2Y8n-3xNwAbRsQyTaygfppJGiWhpdJyQVPlW2cBdSgYXk5-vx_vHEW7Yz6-dIu_5YcYNtxQM5r5GhX8TNutJWmo-jJFCkKGlFFZehWuRbGrD2HRIVsuuZIm4BoSDdHYj8Y9baPPtlbzr5qlJdZcsUarALaxQKPbIPq2t44np5sXM7mpFr_QOv5P5-7ArQ6eku1Wnu7CFVPdgxt5HxXuPnw9Lp0STQzZw1X9j2_fMfaHMpp8Dl-yE4J0_a13HTk07Z0JMrVke3KKcyrBXV9yXFZzV8Wi1KZ-Rdo5l3ycVw6K1mWNyUfO2LZ7lOXCFX0wP0cnyPoBHI3efMp3aBfAgSoHS1LKDZfShMZXgdDuESoKjZZxJBgXkXYykvg6iJRkcSi1tVzxQFolsNfG4bLwIaxV08o8AhIzqbiTIpskwoGKJOPM-iFTWeSWRDo1HtD-_xWqYzfHIBuTouVlZgUOaTEMqQcvhvRnLa_Hb1Ou9-JQdPpdF3j6nLnJkPsebFwWkaGw5syRIT9ic4DiQfA3yfKu6UhIMPOANTLyhwYW-e6HfHh7_C-ZnsP1g9ejYu_t_rsncNN9Rs8kGvB1WJudX5inDnfN5LNGtX4Ca-wlDQ |
| 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=Visible+Light%E2%80%90Induced+Annulation+Reaction+of+Alkenes+with+Vinyl+Azides%3A+Direct+Synthesis+of+Functionalized+Pyrroles&rft.jtitle=Chinese+journal+of+chemistry&rft.au=Yang%2C+Ming&rft.au=Xin%E2%80%90Yu+Wang&rft.au=Wang%2C+Jie&rft.au=Yu%E2%80%90Long+Zhao&rft.date=2024-01-15&rft.pub=Wiley+Subscription+Services%2C+Inc&rft.issn=1001-604X&rft.eissn=1614-7065&rft.volume=42&rft.issue=2&rft.spage=151&rft.epage=156&rft_id=info:doi/10.1002%2Fcjoc.202300498&rft.externalDBID=NO_FULL_TEXT |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1001-604X&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1001-604X&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1001-604X&client=summon |