DSpace at EWHA: N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction

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DC Field	Value	Language
dc.contributor.author	김성각	-
dc.date.accessioned	2016-08-28T11:08:48Z	-
dc.date.available	2016-08-28T11:08:48Z	-
dc.date.issued	2001	-
dc.identifier.issn	0936-5214	-
dc.identifier.other	OAK-842	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/218872	-
dc.description.abstract	N-Alkoxyimidoyl bromides have been successfully employed as an efficient organic partner in the Pd-catalyzed Stille coupling reaction with various organotin compounds, and the corresponding O-alkyloximes were obtained in good to excellent yields.	-
dc.language	English	-
dc.title	N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction	-
dc.type	Article	-
dc.relation.issue	10	-
dc.relation.index	SCIE	-
dc.relation.index	SCOPUS	-
dc.relation.startpage	1557	-
dc.relation.lastpage	1558	-
dc.relation.journaltitle	Synlett	-
dc.identifier.wosid	WOS:000171453000016	-
dc.identifier.scopusid	2-s2.0-0034805839	-
dc.author.google	Chang S.	-
dc.author.google	Lee M.	-
dc.author.google	Kim S.	-
dc.date.modifydate	20160718162637	-