DSpace at EWHA: Copper-catalyzed N-arylation of tert-butyl N-sulfonylcarbamates with diaryliodonium salts at room temperature

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DC Field	Value	Language
dc.contributor.author	김원석	*
dc.date.accessioned	2016-08-27T04:08:16Z	-
dc.date.available	2016-08-27T04:08:16Z	-
dc.date.issued	2015	*
dc.identifier.issn	0040-4020	*
dc.identifier.other	OAK-14671	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/217075	-
dc.description.abstract	A new and mild synthetic approach for the synthesis of N-arylsulfonamides under copper-catalyzed conditions at room temperature has been developed. The reaction employs various tert-butyl N-sulfonylcarbamates and diaryliodonium salts to avoid potential genotoxic impurities. A one-pot coupling/Boc-deprotection sequence is also reported to provide mono N-arylsulfonamides in good to excellent yields. © 2015 Elsevier Ltd.	*
dc.language	English	*
dc.publisher	Elsevier Ltd	*
dc.subject	Copper catalysis	*
dc.subject	Diaryliodonium salts	*
dc.subject	Mono N-arylsulfonamides	*
dc.subject	Room temperature	*
dc.subject	Tert-Butyl N-sulfonylcarbamates	*
dc.title	Copper-catalyzed N-arylation of tert-butyl N-sulfonylcarbamates with diaryliodonium salts at room temperature	*
dc.type	Article in Press	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.journaltitle	Tetrahedron	*
dc.identifier.doi	10.1016/j.tet.2015.01.032	*
dc.identifier.wosid	WOS:000351320900010	*
dc.identifier.scopusid	2-s2.0-84922205238	*
dc.author.google	Moon S.-Y.	*
dc.author.google	Koh M.	*
dc.author.google	Rathwell K.	*
dc.author.google	Jung S.-H.	*
dc.author.google	Kim W.-S.	*
dc.contributor.scopusid	김원석(57203484044)	*
dc.date.modifydate	20240220102223	*