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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

Nickel/Briphos-Catalyzed Direct Transamidation of Unactivated Secondary Amides Using Trimethylsilyl Chloride

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dc.contributor.authorYu, Subeenko
dc.contributor.authorShin, TaeIlko
dc.contributor.authorZhang, Maoshengko
dc.contributor.authorXia, Yuanzhiko
dc.contributor.authorKim, Hyunwooko
dc.contributor.authorLee, Sunwooko
dc.date.accessioned2019-01-22T08:31:05Z-
dc.date.available2019-01-22T08:31:05Z-
dc.date.created2018-12-26-
dc.date.created2018-12-26-
dc.date.created2018-12-26-
dc.date.issued2018-12-
dc.identifier.citationORGANIC LETTERS, v.20, no.23, pp.7563 - 7566-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10203/249007-
dc.description.abstractDirect transamidation of secondary amides was developed via nickel catalysis. In the presence of trimethylsilyl chloride and manganese, Ni(diglyme)Cl-2 with a Briphos ligand efficiently promoted the transamidation of N-aryl benzamide derivatives with primary amines to afford the corresponding secondary amides in moderate to good yields. Primary amines bearing electron-donating groups gave higher yields of the transamidation products.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleNickel/Briphos-Catalyzed Direct Transamidation of Unactivated Secondary Amides Using Trimethylsilyl Chloride-
dc.typeArticle-
dc.identifier.wosid000452930100047-
dc.identifier.scopusid2-s2.0-85058378000-
dc.type.rimsART-
dc.citation.volume20-
dc.citation.issue23-
dc.citation.beginningpage7563-
dc.citation.endingpage7566-
dc.citation.publicationnameORGANIC LETTERS-
dc.identifier.doi10.1021/acs.orglett.8b03304-
dc.contributor.localauthorKim, Hyunwoo-
dc.contributor.nonIdAuthorYu, Subeen-
dc.contributor.nonIdAuthorZhang, Maosheng-
dc.contributor.nonIdAuthorXia, Yuanzhi-
dc.contributor.nonIdAuthorLee, Sunwoo-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusPD-NHC PRECATALYST-
dc.subject.keywordPlusCARBOXYLIC-ACIDS-
dc.subject.keywordPlusGENERAL-METHOD-
dc.subject.keywordPlusESTERS-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusDISCOVERY-
dc.subject.keywordPlusLIGANDS-
dc.subject.keywordPlusPEPPSI-
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