DSpace at EWHA: Synthesis of 1,3-Dialkyl-1,2,3-triazolium ionic liquids and their applications to the baylis-hillman reaction

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DC Field	Value	Language
dc.contributor.author	류재상	*
dc.date.accessioned	2016-08-28T12:08:19Z	-
dc.date.available	2016-08-28T12:08:19Z	-
dc.date.issued	2010	*
dc.identifier.issn	0022-3263	*
dc.identifier.other	OAK-6618	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/220826	-
dc.description.abstract	Novel 1,3-dialkyl-1,2,3-triazolium ionic liquids were synthesized via click reactions using 1-trimethylsilylacetylene and alkyl azides and were efficient reaction media for the Baylis-Hillman reaction. The problems associated with deprotonation of the C-2 hydrogen of [bmim][PF6] could be suppressed in the reaction of [bmTr][PF6] or [bmTr][NTf2]. 1,3-Dialkyl-1,2,3-triazolium ionic liquids are chemically inert under basic conditions and more suitable media for the reactions involving bases than the common 1,3-dialkylimidazolium ionic liquids. © 2010 American Chemical Society.	*
dc.language	English	*
dc.title	Synthesis of 1,3-Dialkyl-1,2,3-triazolium ionic liquids and their applications to the baylis-hillman reaction	*
dc.type	Article	*
dc.relation.issue	12	*
dc.relation.volume	75	*
dc.relation.index	SCI	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	4183	*
dc.relation.lastpage	4191	*
dc.relation.journaltitle	Journal of Organic Chemistry	*
dc.identifier.doi	10.1021/jo100618d	*
dc.identifier.wosid	WOS:000278560700026	*
dc.identifier.scopusid	2-s2.0-77953507131	*
dc.author.google	Jeong Y.	*
dc.author.google	Ryu J.-S.	*
dc.contributor.scopusid	류재상(36081118200)	*
dc.date.modifydate	20231120165709	*