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분자활성촉매반응연구단
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A Direct Access to 7-Aminoindoles via Iridium-Catalyzed Mild C-H Amidation of N-Pivaloylindoles with Organic Azides

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dc.contributor.authorYouyoung Kim-
dc.contributor.authorJuhyeon Park-
dc.contributor.authorSukbok Chang-
dc.date.available2016-07-06T02:47:42Z-
dc.date.created2016-06-20-
dc.date.issued2016-04-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/2641-
dc.description.abstractIr(III)-catalyzed regioselective direct C-7 amidation of indoles in reaction with organic azides has been developed. While its efficiency was varied by the choice of N-directing groups, N-pivaloylindoles were most effective in undergoing the desired amidation at room temperature over a broad range of substrates. The reaction was scalable, and deprotection of the chelation group was also facile. © 2016 American Chemical Society-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleA Direct Access to 7-Aminoindoles via Iridium-Catalyzed Mild C-H Amidation of N-Pivaloylindoles with Organic Azides-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000374436800046-
dc.identifier.scopusid2-s2.0-84966292059-
dc.identifier.rimsid55865ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorYouyoung Kim-
dc.contributor.affiliatedAuthorJuhyeon Park-
dc.contributor.affiliatedAuthorSukbok Chang-
dc.identifier.doi10.1021/acs.orglett.6b00662-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.18, no.8, pp.1892 - 1895-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume18-
dc.citation.number8-
dc.citation.startPage1892-
dc.citation.endPage1895-
dc.date.scptcdate2018-10-01-
dc.description.wostc35-
dc.description.scptc37-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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