DSpace at EWHA: Tandem blaise-alkenylation with unactivated alkynes: One-pot synthesis of α-vinylated β-enaminoesters from nitriles

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DC Field	Value	Language
dc.contributor.author	이상기	*
dc.contributor.author	전유성	*
dc.date.accessioned	2016-08-29T11:08:13Z	-
dc.date.available	2016-08-29T11:08:13Z	-
dc.date.issued	2009	*
dc.identifier.issn	1523-7060	*
dc.identifier.other	OAK-5789	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/232013	-
dc.description.abstract	The in situ generated Blaise reaction intermediate, a zinc bromide complex of β-enaminoester, reacts with various unactivated terminal alkynes and an internal alkyne under mild conditions to afford α-vinylated β-enaminoesters in good to excellent yields. © 2009 American Chemical Society.	*
dc.language	English	*
dc.title	Tandem blaise-alkenylation with unactivated alkynes: One-pot synthesis of α-vinylated β-enaminoesters from nitriles	*
dc.type	Article	*
dc.relation.issue	15	*
dc.relation.volume	11	*
dc.relation.index	SCI	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	3414	*
dc.relation.lastpage	3417	*
dc.relation.journaltitle	Organic Letters	*
dc.identifier.doi	10.1021/ol901241s	*
dc.identifier.wosid	WOS:000268479900064	*
dc.identifier.scopusid	2-s2.0-68149087630	*
dc.author.google	Chun Y.S.	*
dc.author.google	Ko Y.O.	*
dc.author.google	Shin H.	*
dc.author.google	Lee S.-G.	*
dc.contributor.scopusid	이상기(15082786300)	*
dc.contributor.scopusid	전유성(57263448400)	*
dc.date.modifydate	20240405124818	*