Transition-metal-catalyzed additions of C-H bonds to C-X (X = N, O) multiple bonds via C-H bond activation
Chemical transformations via catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry. Transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitri...
Saved in:
Published in | Organic & biomolecular chemistry Vol. 11; no. 34; pp. 5558 - 5578 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
14.09.2013
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Chemical transformations
via
catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry. Transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide, have undergone a rapid development in recent years. In this review, recent advances in this active area have been highlighted and their mechanisms have been discussed.
A review highlighting recent advances and mechanisms of transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide. |
---|---|
AbstractList | Chemical transformations via catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry. Transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide, have undergone a rapid development in recent years. In this review, recent advances in this active area have been highlighted and their mechanisms have been discussed. Chemical transformations via catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry. Transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide, have undergone a rapid development in recent years. In this review, recent advances in this active area have been highlighted and their mechanisms have been discussed.Chemical transformations via catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry. Transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide, have undergone a rapid development in recent years. In this review, recent advances in this active area have been highlighted and their mechanisms have been discussed. Chemical transformations via catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry. Transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide, have undergone a rapid development in recent years. In this review, recent advances in this active area have been highlighted and their mechanisms have been discussed. A review highlighting recent advances and mechanisms of transition-metal-catalyzed addition reactions of C-H bonds to polar C-X (X = N, O) multiple bonds, such as aldehydes, ketones, imines, isocyanates, nitriles, isocyanides, carbon monoxide and carbon dioxide. |
Author | Yang, Minghua Yan, Guobing Wu, Xiangmei |
AuthorAffiliation | Department of Chemistry Lishui University |
AuthorAffiliation_xml | – name: Lishui University – name: Department of Chemistry |
Author_xml | – sequence: 1 givenname: Guobing surname: Yan fullname: Yan, Guobing – sequence: 2 givenname: Xiangmei surname: Wu fullname: Wu, Xiangmei – sequence: 3 givenname: Minghua surname: Yang fullname: Yang, Minghua |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23851628$$D View this record in MEDLINE/PubMed |
BookMark | eNp90c1LwzAUAPAgE50fF-9KvKlYTdo0SQ8eZKgTRC8Ku4XXNIFo28wmE_Svt3NzgoiXJI_3ew9e3hYatL41CO1RckZJVpzrzJeM8Dx9WUNDyoRISJ4Vg9U7JZtoK4RnQmghONtAm2kmc8pTOUTPjx20wUXn26QxEepEQ3--f5gKQ1V9JQL2Fo-SMS59WwUcfR9M8NEEX-D7U_xwjJtZHd20Nkvw5mDFMejo3mDeZgetW6iD2V3e2-jp-upxNE7uHm5uR5d3iWaExiSXTBTCAhgmC57bitlcVzQVQgCUlEJppZYEuDA60zzlElLORVmkhZVC2GwbHS36Tjv_OjMhqsYFbeoaWuNnQVFGJWe5FKynB0s6KxtTqWnnGuje1ff_9IAsgO58CJ2xSrv4NU3swNWKEjVfgfpZQV9y8qvku-uf-HCBu6BX7ievptV8nv3_TPYJNnWaIQ |
CitedBy_id | crossref_primary_10_1002_cjoc_202200553 crossref_primary_10_1002_tcr_201500250 crossref_primary_10_6023_cjoc202204056 crossref_primary_10_1055_a_2114_5426 crossref_primary_10_1021_ja511964k crossref_primary_10_1002_ejoc_201500329 crossref_primary_10_1016_j_tet_2015_02_062 crossref_primary_10_1039_C5DT00032G crossref_primary_10_1016_S1872_2067_15_60872_5 crossref_primary_10_1021_acs_orglett_0c01052 crossref_primary_10_1021_ol500186j crossref_primary_10_1021_acs_joc_4c01581 crossref_primary_10_1021_acs_chemrev_6b00661 crossref_primary_10_1002_anie_202016027 crossref_primary_10_1002_chem_202103319 crossref_primary_10_1039_C4OB01596G crossref_primary_10_1021_acs_orglett_6b02460 crossref_primary_10_1002_adsc_201600297 crossref_primary_10_1002_ange_201608715 crossref_primary_10_1002_adsc_201400984 crossref_primary_10_1021_acs_joc_9b01237 crossref_primary_10_1021_acs_orglett_5b00938 crossref_primary_10_1039_C6OB00108D crossref_primary_10_1002_cssc_201802012 crossref_primary_10_1021_acs_orglett_5b00027 crossref_primary_10_1002_ejoc_201700358 crossref_primary_10_1021_ja501910e crossref_primary_10_1016_S1872_2067_14_60245_X crossref_primary_10_1039_C4CC08407A crossref_primary_10_1002_ijch_201700021 crossref_primary_10_1002_ejoc_201403203 crossref_primary_10_1002_adsc_201300865 crossref_primary_10_1016_j_tet_2016_03_004 crossref_primary_10_1021_acscatal_8b00680 crossref_primary_10_1002_ange_201503149 crossref_primary_10_1002_adsc_201500768 crossref_primary_10_1002_ajoc_202100299 crossref_primary_10_1039_C5SC04138D crossref_primary_10_1002_ejic_201901016 crossref_primary_10_1002_ejoc_202000071 crossref_primary_10_1021_acs_orglett_6b02848 crossref_primary_10_1021_acs_orglett_6b01072 crossref_primary_10_1021_acs_organomet_9b00087 crossref_primary_10_1021_acs_joc_5b00059 crossref_primary_10_1021_cr500610p crossref_primary_10_1002_anie_201503149 crossref_primary_10_1039_D2QO00389A crossref_primary_10_1002_ange_202016027 crossref_primary_10_1021_acs_joc_2c01908 crossref_primary_10_1002_anie_201400147 crossref_primary_10_1002_adsc_201500709 crossref_primary_10_1021_acs_joc_2c02039 crossref_primary_10_1002_asia_202001219 crossref_primary_10_1021_ol403166p crossref_primary_10_1021_acs_organomet_3c00418 crossref_primary_10_1002_anie_201608715 crossref_primary_10_1039_D4OB00689E crossref_primary_10_1246_bcsj_20150180 crossref_primary_10_1021_jacs_8b03998 crossref_primary_10_1246_cl_140452 crossref_primary_10_1002_ange_201506437 crossref_primary_10_1039_C3SC53115E crossref_primary_10_1039_C4RA17182A crossref_primary_10_1021_acs_orglett_9b02142 crossref_primary_10_1039_C4CC03627A crossref_primary_10_1021_acs_orglett_6b02146 crossref_primary_10_1007_s11426_014_5130_y crossref_primary_10_1002_chem_201900762 crossref_primary_10_1016_j_tet_2020_131079 crossref_primary_10_1039_C6QO00059B crossref_primary_10_1002_cctc_201600433 crossref_primary_10_1002_anie_201506437 crossref_primary_10_1002_chem_201501449 crossref_primary_10_1002_asia_202100797 crossref_primary_10_1021_acscatal_1c03153 crossref_primary_10_1002_chin_201344232 crossref_primary_10_1039_C8QO00932E crossref_primary_10_1002_ange_201603831 crossref_primary_10_1016_j_jorganchem_2021_121973 crossref_primary_10_1039_c3ra44486d crossref_primary_10_1039_C6CC02468H crossref_primary_10_1021_ja5116452 crossref_primary_10_1021_acs_orglett_1c01083 crossref_primary_10_1021_ol4025309 crossref_primary_10_1021_cs501924c crossref_primary_10_1055_a_1683_9455 crossref_primary_10_1016_j_cclet_2016_05_011 crossref_primary_10_1016_j_tet_2016_10_004 crossref_primary_10_1016_j_tet_2019_07_008 crossref_primary_10_1039_D0NJ03721D crossref_primary_10_1002_ange_201400147 crossref_primary_10_1021_jacs_7b02775 crossref_primary_10_1246_bcsj_20200352 crossref_primary_10_1021_acs_orglett_7b02871 crossref_primary_10_1016_j_tet_2018_03_007 crossref_primary_10_1002_anie_201603831 crossref_primary_10_1016_j_tetlet_2014_04_016 crossref_primary_10_1039_D0OB02309D crossref_primary_10_1002_cctc_201500213 crossref_primary_10_1021_acs_orglett_5b00910 crossref_primary_10_5059_yukigoseikyokaishi_76_604 |
Cites_doi | 10.1007/128_2009_12 10.1002/adsc.201200909 10.1021/cr800421c 10.1002/chem.201001363 10.1055/s-0030-1260981 10.1021/cr020007u 10.1039/b805701j 10.1002/anie.200702256 10.1002/chem.200900281 10.1021/ol200684b 10.1039/b816707a 10.1021/ol4003674 10.1021/ja308976x 10.1021/ol301760n 10.1002/anie.201002031 10.1002/adsc.201000556 10.1039/c3cs35507a 10.1021/cr00104a001 10.1021/ol103150g 10.1021/cr100280d 10.1002/anie.201201050 10.1002/anie.201007464 10.1021/ar9002587 10.1021/ar200206a 10.1021/ja3083494 10.1039/c1cs15083a 10.1002/anie.201003995 10.1002/anie.200903505 10.1039/c1cs15109f 10.1039/C0CS00098A 10.1021/ja910104n 10.1246/cl.2007.872 10.1002/anie.201004153 10.1007/3-540-68525-1_3 10.1021/ja3036459 10.1002/anie.201209226 10.1021/ar200190g 10.1021/ol8021512 10.1021/cr900184e 10.1002/chem.201100736 10.1021/ja038687l 10.1002/adsc.201200690 10.1002/anie.200300590 10.1021/ol302000a 10.1002/(SICI)1521-3773(19990614)38:12<1698::AID-ANIE1698>3.0.CO;2-6 10.1021/cr980414z 10.1021/jo060220g 10.1021/cr100379j 10.1021/cr0104330 10.1002/1521-3773(20020802)41:15<2779::AID-ANIE2779>3.0.CO;2-J 10.1021/cr078370u 10.1021/ja203495c 10.1021/ol2032784 10.1039/c2sc20835k 10.1021/ja103429q 10.1002/adsc.201100232 10.1021/cr900005n 10.1021/ja065643e 10.1021/ja9036669 10.1002/(SICI)1099-0682(199907)1999:7<1047::AID-EJIC1047>3.0.CO;2-B 10.1021/ar300014f 10.1039/c2cs15281a 10.1002/anie.200703382 10.1021/cr1004474 10.1016/j.tet.2011.01.086 10.1016/j.tet.2007.05.083 10.1039/C2CC36817J 10.1021/ol200638z 10.1021/ol303440y 10.1021/ja054216i 10.1021/ol900962v 10.1039/C0SC00419G 10.1002/anie.201100763 10.1021/ja211110h 10.1016/j.ccr.2009.07.023 10.1039/C1CS15104E 10.1039/c2cc31114c 10.1002/anie.201103945 10.1016/j.tet.2008.01.145 10.1021/ol301989n 10.1002/adsc.200900570 10.1002/anie.201207995 10.1021/cr300153j 10.1002/(SICI)1521-3773(19981217)37:23<3279::AID-ANIE3279>3.0.CO;2-M 10.1021/ja109097z 10.1246/cl.1978.535 10.1055/s-0031-1291041 10.1039/c1cc15781g 10.1021/cr100198w 10.1039/c0cs00125b 10.1021/ol801070n 10.1021/ja109562x 10.1021/ol300723x 10.1021/ja203875d 10.1021/cr020022z |
ContentType | Journal Article |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1039/c3ob40652k |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1477-0539 |
EndPage | 5578 |
ExternalDocumentID | 23851628 10_1039_c3ob40652k c3ob40652k |
Genre | Research Support, Non-U.S. Gov't Journal Article Review |
GroupedDBID | --- -DZ -~X 0-7 0R~ 0UZ 123 186 1TJ 29N 3EH 4.4 53G 6TJ 705 70~ 71~ 7~J 9M8 AAEMU AAIWI AAJAE AAMEH AANOJ AAWGC AAXHV AAXPP AAYXX ABASK ABDVN ABEMK ABJNI ABPDG ABRYZ ABXOH ACGFS ACHDF ACIWK ACLDK ACNCT ACPRK ACRPL ADMRA ADNMO ADSRN AEFDR AENEX AENGV AESAV AETIL AFFNX AFLYV AFOGI AFRAH AFRDS AFRZK AFVBQ AGEGJ AGKEF AGQPQ AGRSR AHGCF AHGXI AKMSF ALMA_UNASSIGNED_HOLDINGS ALSGL ALUYA ANBJS ANLMG ANUXI APEMP ASKNT ASPBG AUDPV AVWKF AZFZN BBWZM BLAPV BSQNT C6K CAG CITATION COF CS3 D0L DU5 EBS ECGLT EE0 EEHRC EF- EJD F5P FEDTE GGIMP GNO H13 HVGLF HZ~ H~N IDY IDZ J3G J3H J3I L-8 M4U MVM N9A NDZJH O9- P2P R56 R7B R7C RAOCF RCLXC RCNCU RNS ROL RPMJG RRA RRC RSCEA SKA SKF SLH TN5 TWZ UQL VH6 WH7 XJT XOL XSW YNT YZZ ZCG -JG AGSTE CGR CUY CVF ECM EIF NPM OK1 UCJ VQA 7X8 |
ID | FETCH-LOGICAL-c401t-584797faae48965fd4f5cd12777aab11abf8c80a67ec3c6268a2667b929f877f3 |
ISSN | 1477-0520 1477-0539 |
IngestDate | Fri Jul 11 09:17:17 EDT 2025 Wed Feb 19 01:52:03 EST 2025 Thu Apr 24 22:52:01 EDT 2025 Tue Jul 01 00:22:49 EDT 2025 Thu May 19 04:22:22 EDT 2016 Sat Jun 01 02:22:46 EDT 2019 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 34 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c401t-584797faae48965fd4f5cd12777aab11abf8c80a67ec3c6268a2667b929f877f3 |
Notes | Minghua Yang was born in 1971, in Hunan, China. He obtained his B.Sc. degree in chemistry from Hubei Normal University and M.Sc. degree from the Hubei University (China). He received his Ph.D. degree from Nanjing University in 2005 under the supervision of Chengjiang Zhu and Yi Pan, and then entered Lishui University as an associate professor. In 2006, He joined Dr Liu's group at the University of Macquarie (Australia) as a visiting professor and then returned to Lishui University in 2007, where he is still working today. He became a professor in 2010. Apart from the development of asymmetric reactions for obtaining chiral organochalcogenide compounds, his research interests include the transition-metal-catalyzed formation of carbon-carbon and carbon-heteroatom bonds. Xiangmei Wu was born in Zhejiang, China, in 1971. She obtained her B.Sc. degree from Zhejiang Normal University. Her M.Sc. degree was obtained from Zhejiang University of Technology in 2005, followed by her Ph.D. degree in 2009. She has been at Lishui University since 1993. She became a professor in 2009. Her current research interests focus on the transition-metal-catalyzed formation of carbon-carbon and carbon-heteroatom bonds and green synthetic chemistry. Guobing Yan was born in 1975, in Jiangxi, China. He obtained his B.Sc. degree from Jinggangshan University, his M.Sc. degree from Suzhou University, and his Ph.D. degree from Tongji University in 2010. He spent two years in 2008 and 2009 as visiting student in Professor Jianbo Wang's laboratory at Peking University. He has been at Lishui University since 2010 as an associate professor. His current research interests focus on the transition-metal-catalyzed activation of inert chemical bonds and green synthetic chemistry. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
PMID | 23851628 |
PQID | 1418645874 |
PQPubID | 23479 |
PageCount | 21 |
ParticipantIDs | crossref_citationtrail_10_1039_c3ob40652k crossref_primary_10_1039_c3ob40652k rsc_primary_c3ob40652k pubmed_primary_23851628 proquest_miscellaneous_1418645874 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2013-09-14 |
PublicationDateYYYYMMDD | 2013-09-14 |
PublicationDate_xml | – month: 09 year: 2013 text: 2013-09-14 day: 14 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Organic & biomolecular chemistry |
PublicationTitleAlternate | Org Biomol Chem |
PublicationYear | 2013 |
References | Jiang (c3ob40652k-(cit49)/*[position()=1]) 2013; 15 Thansandote (c3ob40652k-(cit4p)/*[position()=1]) 2009; 15 Ritleng (c3ob40652k-(cit3d)/*[position()=1]) 2002; 102 Shi (c3ob40652k-(cit31c)/*[position()=1]) 2011; 40 Hou (c3ob40652k-(cit46)/*[position()=1]) 2013; 15 Ramirez (c3ob40652k-(cit4e)/*[position()=1]) 2012; 41 Yamada (c3ob40652k-(cit21a)/*[position()=1]) 2008; 108 Kuninobu (c3ob40652k-(cit12)/*[position()=1]) 2009; 11 Hayashi (c3ob40652k-(cit7b)/*[position()=1]) 2003; 103 Takaya (c3ob40652k-(cit48)/*[position()=1]) 2009; 131 Kuninobu (c3ob40652k-(cit9)/*[position()=1]) 2006; 128 Ritleng (c3ob40652k-(cit5d)/*[position()=1]) 2002; 102 Gao (c3ob40652k-(cit29)/*[position()=1]) 2012; 48 Fukumoto (c3ob40652k-(cit8)/*[position()=1]) 2002; 41 Colby (c3ob40652k-(cit5b)/*[position()=1]) 2010; 110 Aydin (c3ob40652k-(cit32)/*[position()=1]) 2008; 10 Satoh (c3ob40652k-(cit5c)/*[position()=1]) 2010; 16 Shibata (c3ob40652k-(cit20)/*[position()=1]) 2011 Sun (c3ob40652k-(cit4g)/*[position()=1]) 2011; 111 Fagnou (c3ob40652k-(cit7a)/*[position()=1]) 2003; 103 Guan (c3ob40652k-(cit55)/*[position()=1]) 2012; 134 Kuninobu (c3ob40652k-(cit11)/*[position()=1]) 2007; 46 Hartwig (c3ob40652k-(cit4c)/*[position()=1]) 2012; 45 Kuninobu (c3ob40652k-(cit42)/*[position()=1]) 2007; 36 Kakiuchi (c3ob40652k-(cit3a)/*[position()=1]) 1999; 3 Dyker (c3ob40652k-(cit3c)/*[position()=1]) 1999; 38 Xie (c3ob40652k-(cit58)/*[position()=1]) 2012; 134 Guari (c3ob40652k-(cit3b)/*[position()=1]) 1999 Lyons (c3ob40652k-(cit4k)/*[position()=1]) 2010; 110 Wendlandt (c3ob40652k-(cit31a)/*[position()=1]) 2011; 50 Komai (c3ob40652k-(cit38)/*[position()=1]) 2012; 44 Bouffard (c3ob40652k-(cit4l)/*[position()=1]) 2010; 292 Rohbogner (c3ob40652k-(cit2c)/*[position()=1]) 2008; 47 Tsuchikama (c3ob40652k-(cit19)/*[position()=1]) 2009; 351 Whisler (c3ob40652k-(cit2b)/*[position()=1]) 2004; 43 Jaric (c3ob40652k-(cit2e)/*[position()=1]) 2010; 49 Yus (c3ob40652k-(cit7c)/*[position()=1]) 2011; 111 Tauchert (c3ob40652k-(cit23)/*[position()=1]) 2012; 134 Arockiam (c3ob40652k-(cit4a)/*[position()=1]) 2012; 112 Aydin (c3ob40652k-(cit33)/*[position()=1]) 2008; 10 Neufeldt (c3ob40652k-(cit4b)/*[position()=1]) 2012; 45 Zhang (c3ob40652k-(cit61)/*[position()=1]) 2010; 49 Giri (c3ob40652k-(cit4n)/*[position()=1]) 2009; 38 Yeung (c3ob40652k-(cit4f)/*[position()=1]) 2011; 111 Yang (c3ob40652k-(cit13)/*[position()=1]) 2011; 353 Zhou (c3ob40652k-(cit47b)/*[position()=1]) 2006; 71 Li (c3ob40652k-(cit24)/*[position()=1]) 2011; 50 Sadjadi (c3ob40652k-(cit50)/*[position()=1]) 2011; 67 Yeung (c3ob40652k-(cit31d)/*[position()=1]) 2011; 111 Colby (c3ob40652k-(cit5a)/*[position()=1]) 2012; 45 Inomata (c3ob40652k-(cit62)/*[position()=1]) 2012; 14 Hong (c3ob40652k-(cit40)/*[position()=1]) 1978 Wu (c3ob40652k-(cit52)/*[position()=1]) 2011; 40 Yoshino (c3ob40652k-(cit30)/*[position()=1]) 2013; 52 Hesp (c3ob40652k-(cit25)/*[position()=1]) 2012; 14 Wunderlich (c3ob40652k-(cit2d)/*[position()=1]) 2009; 48 Wencel-Delord (c3ob40652k-(cit4h)/*[position()=1]) 2011; 40 Hopkinson (c3ob40652k-(cit4j)/*[position()=1]) 2011; 17 Chen (c3ob40652k-(cit57)/*[position()=1]) 2011; 47 Shi (c3ob40652k-(cit17)/*[position()=1]) 2012; 354 Zhou (c3ob40652k-(cit47a)/*[position()=1]) 2004; 126 Li (c3ob40652k-(cit21c)/*[position()=1]) 2010; 43 Qian (c3ob40652k-(cit35)/*[position()=1]) 2010; 352 Liu (c3ob40652k-(cit53)/*[position()=1]) 2011; 50 Sakai (c3ob40652k-(cit6)/*[position()=1]) 1998; 37 Lian (c3ob40652k-(cit16)/*[position()=1]) 2012; 3 Li (c3ob40652k-(cit14)/*[position()=1]) 2011; 2 Zhang (c3ob40652k-(cit64)/*[position()=1]) 2011; 13 Chiusoli (c3ob40652k-(cit4m)/*[position()=1]) 2010; 254 Boorman (c3ob40652k-(cit4i)/*[position()=1]) 2011; 40 Rueping (c3ob40652k-(cit37)/*[position()=1]) 2011; 13 Song (c3ob40652k-(cit4d)/*[position()=1]) 2012; 41 Gawronski (c3ob40652k-(cit21b)/*[position()=1]) 2008; 108 Zhang (c3ob40652k-(cit54)/*[position()=1]) 2012; 51 Qiu (c3ob40652k-(cit51)/*[position()=1]) 2013; 42 Liang (c3ob40652k-(cit56)/*[position()=1]) 2013; 49 Kuninobu (c3ob40652k-(cit41)/*[position()=1]) 2006; 128 Kuninobu (c3ob40652k-(cit10)/*[position()=1]) 2007; 63 Qian (c3ob40652k-(cit34)/*[position()=1]) 2010; 132 Mizuno (c3ob40652k-(cit63)/*[position()=1]) 2011; 133 McGlacken (c3ob40652k-(cit4o)/*[position()=1]) 2009; 38 Boogaerts (c3ob40652k-(cit59)/*[position()=1]) 2010; 132 Lian (c3ob40652k-(cit27)/*[position()=1]) 2013; 52 Kuninobu (c3ob40652k-(cit43)/*[position()=1]) 2008; 64 Sundararaju (c3ob40652k-(cit18)/*[position()=1]) 2011; 133 Kobayashi (c3ob40652k-(cit1c)/*[position()=1]) 1999; 99 Qian (c3ob40652k-(cit36)/*[position()=1]) 2011; 13 Zhou (c3ob40652k-(cit28)/*[position()=1]) 2013; 355 Hesp (c3ob40652k-(cit44)/*[position()=1]) 2011; 133 Liu (c3ob40652k-(cit31b)/*[position()=1]) 2011; 111 Best (c3ob40652k-(cit39)/*[position()=1]) 2012; 134 Snieckus (c3ob40652k-(cit2a)/*[position()=1]) 1990; 90 Tsai (c3ob40652k-(cit22)/*[position()=1]) 2011; 133 Li (c3ob40652k-(cit26)/*[position()=1]) 2012; 14 Li (c3ob40652k-(cit15)/*[position()=1]) 2012; 14 Muralirajan (c3ob40652k-(cit45)/*[position()=1]) 2012; 14 Boogaerts (c3ob40652k-(cit60)/*[position()=1]) 2010; 49 |
References_xml | – issn: 2000 publication-title: Grignard Reagents: New Development doi: Richey – issn: 1996 publication-title: Handbook of Grignard Reagents doi: Silverman Rakita – volume: 292 start-page: 231 year: 2010 ident: c3ob40652k-(cit4l)/*[position()=1] publication-title: Top. Curr. Chem. doi: 10.1007/128_2009_12 – volume: 355 start-page: 360 year: 2013 ident: c3ob40652k-(cit28)/*[position()=1] publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.201200909 – volume: 108 start-page: 5227 year: 2008 ident: c3ob40652k-(cit21b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr800421c – volume: 16 start-page: 11212 year: 2010 ident: c3ob40652k-(cit5c)/*[position()=1] publication-title: Chem.–Eur. J. doi: 10.1002/chem.201001363 – start-page: 2075 year: 2011 ident: c3ob40652k-(cit20)/*[position()=1] publication-title: Synlett doi: 10.1055/s-0030-1260981 – volume: 103 start-page: 169 year: 2003 ident: c3ob40652k-(cit7a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr020007u – volume: 38 start-page: 2447 year: 2009 ident: c3ob40652k-(cit4o)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/b805701j – volume: 46 start-page: 6518 year: 2007 ident: c3ob40652k-(cit11)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200702256 – volume: 15 start-page: 5874 year: 2009 ident: c3ob40652k-(cit4p)/*[position()=1] publication-title: Chem.–Eur. J. doi: 10.1002/chem.200900281 – volume: 13 start-page: 2580 year: 2011 ident: c3ob40652k-(cit36)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol200684b – volume: 38 start-page: 3242 year: 2009 ident: c3ob40652k-(cit4n)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/b816707a – volume: 15 start-page: 1814 year: 2013 ident: c3ob40652k-(cit46)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol4003674 – volume: 134 start-page: 17490 year: 2012 ident: c3ob40652k-(cit55)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja308976x – volume: 14 start-page: 3986 year: 2012 ident: c3ob40652k-(cit62)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol301760n – volume: 49 start-page: 5451 year: 2010 ident: c3ob40652k-(cit2e)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201002031 – volume: 352 start-page: 3195 year: 2010 ident: c3ob40652k-(cit35)/*[position()=1] publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.201000556 – volume: 42 start-page: 5257 year: 2013 ident: c3ob40652k-(cit51)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/c3cs35507a – volume: 90 start-page: 879 year: 1990 ident: c3ob40652k-(cit2a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr00104a001 – volume: 13 start-page: 1095 year: 2011 ident: c3ob40652k-(cit37)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol103150g – volume: 111 start-page: 1215 year: 2011 ident: c3ob40652k-(cit4f)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr100280d – volume: 51 start-page: 5204 year: 2012 ident: c3ob40652k-(cit54)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201201050 – volume: 50 start-page: 2115 year: 2011 ident: c3ob40652k-(cit24)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201007464 – volume: 43 start-page: 581 year: 2010 ident: c3ob40652k-(cit21c)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar9002587 – volume: 111 start-page: 1215 year: 2011 ident: c3ob40652k-(cit31d)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr100280d – volume: 45 start-page: 864 year: 2012 ident: c3ob40652k-(cit4c)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar200206a – volume: 134 start-page: 18193 year: 2012 ident: c3ob40652k-(cit39)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja3083494 – volume: 40 start-page: 4740 year: 2011 ident: c3ob40652k-(cit4h)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/c1cs15083a – volume: 49 start-page: 8670 year: 2010 ident: c3ob40652k-(cit61)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201003995 – volume: 48 start-page: 7256 year: 2009 ident: c3ob40652k-(cit2d)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200903505 – volume: 40 start-page: 4986 year: 2011 ident: c3ob40652k-(cit52)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/c1cs15109f – volume: 40 start-page: 1910 year: 2011 ident: c3ob40652k-(cit4i)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/C0CS00098A – volume: 132 start-page: 3650 year: 2010 ident: c3ob40652k-(cit34)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja910104n – volume: 36 start-page: 872 year: 2007 ident: c3ob40652k-(cit42)/*[position()=1] publication-title: Chem. Lett. doi: 10.1246/cl.2007.872 – volume: 49 start-page: 8674 year: 2010 ident: c3ob40652k-(cit60)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201004153 – volume: 3 start-page: 47 year: 1999 ident: c3ob40652k-(cit3a)/*[position()=1] publication-title: Top. Organomet. Chem. doi: 10.1007/3-540-68525-1_3 – volume: 134 start-page: 9902 year: 2012 ident: c3ob40652k-(cit58)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja3036459 – volume: 52 start-page: 2207 year: 2013 ident: c3ob40652k-(cit30)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201209226 – volume: 45 start-page: 814 year: 2012 ident: c3ob40652k-(cit5a)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar200190g – volume: 10 start-page: 5175 year: 2008 ident: c3ob40652k-(cit33)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol8021512 – volume: 110 start-page: 1147 year: 2010 ident: c3ob40652k-(cit4k)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr900184e – volume: 17 start-page: 8248 year: 2011 ident: c3ob40652k-(cit4j)/*[position()=1] publication-title: Chem.–Eur. J. doi: 10.1002/chem.201100736 – volume: 126 start-page: 2302 year: 2004 ident: c3ob40652k-(cit47a)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja038687l – volume: 354 start-page: 2933 year: 2012 ident: c3ob40652k-(cit17)/*[position()=1] publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.201200690 – volume: 43 start-page: 2206 year: 2004 ident: c3ob40652k-(cit2b)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200300590 – volume: 14 start-page: 4262 year: 2012 ident: c3ob40652k-(cit45)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol302000a – volume: 38 start-page: 1698 year: 1999 ident: c3ob40652k-(cit3c)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/(SICI)1521-3773(19990614)38:12<1698::AID-ANIE1698>3.0.CO;2-6 – volume: 99 start-page: 1069 year: 1999 ident: c3ob40652k-(cit1c)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr980414z – volume: 71 start-page: 3551 year: 2006 ident: c3ob40652k-(cit47b)/*[position()=1] publication-title: J. Org. Chem. doi: 10.1021/jo060220g – volume: 111 start-page: 1780 year: 2011 ident: c3ob40652k-(cit31b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr100379j – volume: 102 start-page: 1731 year: 2002 ident: c3ob40652k-(cit3d)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr0104330 – volume: 41 start-page: 2779 year: 2002 ident: c3ob40652k-(cit8)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/1521-3773(20020802)41:15<2779::AID-ANIE2779>3.0.CO;2-J – volume: 108 start-page: 2874 year: 2008 ident: c3ob40652k-(cit21a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr078370u – volume: 133 start-page: 11430 year: 2011 ident: c3ob40652k-(cit44)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja203495c – volume: 14 start-page: 636 year: 2012 ident: c3ob40652k-(cit15)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol2032784 – volume: 3 start-page: 3088 year: 2012 ident: c3ob40652k-(cit16)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/c2sc20835k – volume: 132 start-page: 8858 year: 2010 ident: c3ob40652k-(cit59)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja103429q – volume: 102 start-page: 1731 year: 2002 ident: c3ob40652k-(cit5d)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr0104330 – volume: 353 start-page: 1269 year: 2011 ident: c3ob40652k-(cit13)/*[position()=1] publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.201100232 – volume: 110 start-page: 624 year: 2010 ident: c3ob40652k-(cit5b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr900005n – volume: 128 start-page: 12376 year: 2006 ident: c3ob40652k-(cit9)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja065643e – volume: 131 start-page: 10824 year: 2009 ident: c3ob40652k-(cit48)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja9036669 – start-page: 1047 year: 1999 ident: c3ob40652k-(cit3b)/*[position()=1] publication-title: Eur. J. Inorg. Chem. doi: 10.1002/(SICI)1099-0682(199907)1999:7<1047::AID-EJIC1047>3.0.CO;2-B – volume: 45 start-page: 936 year: 2012 ident: c3ob40652k-(cit4b)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar300014f – volume: 41 start-page: 3651 year: 2012 ident: c3ob40652k-(cit4d)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/c2cs15281a – volume: 47 start-page: 1503 year: 2008 ident: c3ob40652k-(cit2c)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200703382 – volume: 111 start-page: 7774 year: 2011 ident: c3ob40652k-(cit7c)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr1004474 – volume: 67 start-page: 2707 year: 2011 ident: c3ob40652k-(cit50)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2011.01.086 – volume: 63 start-page: 8463 year: 2007 ident: c3ob40652k-(cit10)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2007.05.083 – volume: 49 start-page: 173 year: 2013 ident: c3ob40652k-(cit56)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C2CC36817J – volume: 13 start-page: 2402 year: 2011 ident: c3ob40652k-(cit64)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol200638z – volume: 15 start-page: 788 year: 2013 ident: c3ob40652k-(cit49)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol303440y – volume: 128 start-page: 202 year: 2006 ident: c3ob40652k-(cit41)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja054216i – volume: 11 start-page: 2711 year: 2009 ident: c3ob40652k-(cit12)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol900962v – volume: 2 start-page: 488 year: 2011 ident: c3ob40652k-(cit14)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/C0SC00419G – volume: 50 start-page: 10788 year: 2011 ident: c3ob40652k-(cit53)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201100763 – volume: 134 start-page: 1482 year: 2012 ident: c3ob40652k-(cit23)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja211110h – volume: 254 start-page: 456 year: 2010 ident: c3ob40652k-(cit4m)/*[position()=1] publication-title: Coord. Chem. Rev. doi: 10.1016/j.ccr.2009.07.023 – volume: 41 start-page: 931 year: 2012 ident: c3ob40652k-(cit4e)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/C1CS15104E – volume: 48 start-page: 4305 year: 2012 ident: c3ob40652k-(cit29)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/c2cc31114c – volume: 50 start-page: 11062 year: 2011 ident: c3ob40652k-(cit31a)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201103945 – volume: 64 start-page: 5974 year: 2008 ident: c3ob40652k-(cit43)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2008.01.145 – volume: 14 start-page: 4498 year: 2012 ident: c3ob40652k-(cit26)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol301989n – volume: 351 start-page: 2850 year: 2009 ident: c3ob40652k-(cit19)/*[position()=1] publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.200900570 – volume: 52 start-page: 629 year: 2013 ident: c3ob40652k-(cit27)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201207995 – volume: 112 start-page: 5879 year: 2012 ident: c3ob40652k-(cit4a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr300153j – volume: 37 start-page: 3279 year: 1998 ident: c3ob40652k-(cit6)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/(SICI)1521-3773(19981217)37:23<3279::AID-ANIE3279>3.0.CO;2-M – volume: 133 start-page: 1251 year: 2011 ident: c3ob40652k-(cit63)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja109097z – start-page: 535 year: 1978 ident: c3ob40652k-(cit40)/*[position()=1] publication-title: Chem. Lett. doi: 10.1246/cl.1978.535 – volume: 44 start-page: 2185 year: 2012 ident: c3ob40652k-(cit38)/*[position()=1] publication-title: Synthesis doi: 10.1055/s-0031-1291041 – volume: 47 start-page: 12224 year: 2011 ident: c3ob40652k-(cit57)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/c1cc15781g – volume: 111 start-page: 1293 year: 2011 ident: c3ob40652k-(cit4g)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr100198w – volume: 40 start-page: 2761 year: 2011 ident: c3ob40652k-(cit31c)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/c0cs00125b – volume: 10 start-page: 2881 year: 2008 ident: c3ob40652k-(cit32)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol801070n – volume: 133 start-page: 1248 year: 2011 ident: c3ob40652k-(cit22)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja109562x – volume: 14 start-page: 2304 year: 2012 ident: c3ob40652k-(cit25)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol300723x – volume: 133 start-page: 10340 year: 2011 ident: c3ob40652k-(cit18)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja203875d – volume: 103 start-page: 2829 year: 2003 ident: c3ob40652k-(cit7b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr020022z |
SSID | ssj0019764 |
Score | 2.4104354 |
SecondaryResourceType | review_article |
Snippet | Chemical transformations
via
catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry.... Chemical transformations via catalytic C-H bond activation have been established as one of the most powerful tools in organic synthetic chemistry.... |
SourceID | proquest pubmed crossref rsc |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 5558 |
SubjectTerms | Aldehydes - chemistry Carbon Dioxide - chemistry Carbon Monoxide - chemistry Catalysis Cyanides - chemistry Imines - chemistry Isocyanates - chemistry Ketones - chemistry Nitriles - chemistry Organic Chemicals - chemical synthesis Organic Chemicals - chemistry Transition Elements - chemistry |
Title | Transition-metal-catalyzed additions of C-H bonds to C-X (X = N, O) multiple bonds via C-H bond activation |
URI | https://www.ncbi.nlm.nih.gov/pubmed/23851628 https://www.proquest.com/docview/1418645874 |
Volume | 11 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxELZCe4AL4lVIecgIDlTBpd6n98ChCoWAoL2k0t4i27FDBd2Nym4leuInIPEP-SWM12vvQoJUuFjJxLY2nln7G88LoadZElOTpZxIFsck0koTFvOIZMLY0bIsEHMTjfzhMJkcR-_yOB8Mvve8lupK7MqLtXEl_8NVoAFfTZTsP3DWTwoE-Az8hRY4DO3leGwOmsbnipwqQNGkuYz5egEg0vgJeSe3sXNpCCcjURofWECcHTE3MBOa8NWoMfofmasC72loB5yf8JVpmkQc5x1rW4xrwztlI1Qmut8V4B1JV1zObzX29vVNbYLQFv58qA0xB7ldnKqTXt-F9fMvFh9r3r-tMJUjMmKjRNsNNkpTYnxv7PnTp9mkRn5Xpj3pa-877R5rMpSt3fz3QpM7VYalAJQSB5-6I86Z9f84-bw_YmOJD7NZN_YK2gxA8YCdc3P_YPr2vbdMAXxrPBXc_3Apb8PsRTf6d5CzorkAjjlz9WUaHDO9ga63Cgjet9J0Ew1UcQtdHTvW3EbLv0sV9lKFS43HP7_9mOBGPHBVNl9z_CzHL_Hhc3y0g50EtV1AgnpDcCc7d9Dx64PpeELauhxEgjZeEWNZz1LNuYoYvOt6HulYzimsV8q5oJQLzSTb40mqZChBY2YcYGAqAIlrlqY63EIbRVmoewgDmGYipIFQPIwyAMsR1alKOFWcJyqgQ7TjFnIm26T1pnbK59kqy4boie-7tKla1vZ67Pgxg4U15jFeqLL-AkowZUkUszQaoruWUX4eALYxTQI2RFvAOU_uT7u9_ofZcq63L_Vk99G17o15gDaqs1o9BMRbiUetEP4ChjanVg |
linkProvider | Royal Society of Chemistry |
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=Transition-metal-catalyzed+additions+of+C%E2%80%93H+bonds+to+C%E2%80%93X+%28X+%3D+N%2C+O%29+multiple+bonds+via+C%E2%80%93H+bond+activation&rft.jtitle=Organic+%26+biomolecular+chemistry&rft.au=Yan%2C+Guobing&rft.au=Wu%2C+Xiangmei&rft.au=Yang%2C+Minghua&rft.date=2013-09-14&rft.issn=1477-0520&rft.eissn=1477-0539&rft.volume=11&rft.issue=34&rft.spage=5558&rft_id=info:doi/10.1039%2Fc3ob40652k&rft.externalDBID=n%2Fa&rft.externalDocID=10_1039_c3ob40652k |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1477-0520&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1477-0520&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1477-0520&client=summon |