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분자활성촉매반응연구단
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Versatile Cp*Co(III)(LX) Catalyst System for Selective Intramolecular C-H Amidation Reactions

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dc.contributor.authorJia Lee-
dc.contributor.authorJeonghyo Lee-
dc.contributor.authorHoimin Jung-
dc.contributor.authorDongwook Kim-
dc.contributor.authorJuhyeon Park-
dc.contributor.authorSukbok Chang-
dc.date.accessioned2020-12-22T02:57:12Z-
dc.date.accessioned2020-12-22T02:57:12Z-
dc.date.available2020-12-22T02:57:12Z-
dc.date.available2020-12-22T02:57:12Z-
dc.date.created2020-09-09-
dc.date.issued2020-07-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/7760-
dc.description.abstract© 2020 American Chemical Society Herein, we report the development of a tailored cobalt catalyst system of Cp*Co(III)(LX) toward intramolecular C-H nitrene insertion of azidoformates to afford cyclic carbamates. The cobalt complexes were easy to prepare and bench-stable, thus offering a convenient reaction protocol. The catalytic reactivity was significantly improved by the electronic tuning of the bidentate LX ligands, and the observed regioselectivity was rationalized by the conformational analysis and DFT calculations of the transition states. The superior performance of the newly developed cobalt catalyst system could be broadly applied to both C(sp2)-H and C(sp3)-H carbamation reactions under mild conditions-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.subjectGAMMA-LACTAMS-
dc.subjectAMINATION-
dc.subjectFUNCTIONALIZATION-
dc.subjectHETEROCYCLES-
dc.subjectDERIVATIVES-
dc.subjectCONVERSION-
dc.subjectINSERTION-
dc.subjectMILD-
dc.subjectARYL-
dc.titleVersatile Cp*Co(III)(LX) Catalyst System for Selective Intramolecular C-H Amidation Reactions-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000551495700047-
dc.identifier.scopusid2-s2.0-85088177591-
dc.identifier.rimsid72826-
dc.contributor.affiliatedAuthorJia Lee-
dc.contributor.affiliatedAuthorJeonghyo Lee-
dc.contributor.affiliatedAuthorHoimin Jung-
dc.contributor.affiliatedAuthorDongwook Kim-
dc.contributor.affiliatedAuthorJuhyeon Park-
dc.contributor.affiliatedAuthorSukbok Chang-
dc.identifier.doi10.1021/jacs.0c04448-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.142, no.28, pp.12324 - 12332-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume142-
dc.citation.number28-
dc.citation.startPage12324-
dc.citation.endPage12332-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusGAMMA-LACTAMS-
dc.subject.keywordPlusAMINATION-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusINSERTION-
dc.subject.keywordPlusMILD-
dc.subject.keywordPlusARYL-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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