DSpace at EWHA: Enantioselective recognition of 1,2-aminoalcohols by the binol receptor dangled with pyrrole-2-carboxamide and its analogues

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DC Field	Value	Language
dc.contributor.author	김관묵	-
dc.date.accessioned	2016-08-29T11:08:51Z	-
dc.date.available	2016-08-29T11:08:51Z	-
dc.date.issued	2009	-
dc.identifier.issn	0040-4020	-
dc.identifier.other	OAK-5353	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/231881	-
dc.description.abstract	Novel binol receptor with pyrrole-2-carboxamide moiety and its analogues have been designed, synthesized, and used to enantioselectively recognize 1,2-aminoalcohols via multiple hydrogen bonding. The pyrrole-based binol receptor showed the highest enantioselectivity among the four receptors as determined by the 1H NMR. The DFT calculation strongly supports complementary hydrogen bonding between alcoholic -OH and pyrrolyl groups. © 2008 Elsevier Ltd. All rights reserved.	-
dc.language	English	-
dc.title	Enantioselective recognition of 1,2-aminoalcohols by the binol receptor dangled with pyrrole-2-carboxamide and its analogues	-
dc.type	Article	-
dc.relation.issue	3	-
dc.relation.volume	65	-
dc.relation.index	SCI	-
dc.relation.index	SCIE	-
dc.relation.index	SCOPUS	-
dc.relation.startpage	666	-
dc.relation.lastpage	671	-
dc.relation.journaltitle	Tetrahedron	-
dc.identifier.doi	10.1016/j.tet.2008.11.022	-
dc.identifier.wosid	WOS:000262773800010	-
dc.identifier.scopusid	2-s2.0-57149122415	-
dc.author.google	Nandhakumar R.	-
dc.author.google	Soo A.Y.	-
dc.author.google	Hong J.	-
dc.author.google	Ham S.	-
dc.author.google	Kim K.M.	-
dc.contributor.scopusid	김관묵(35484385500)	-
dc.date.modifydate	20230208104137	-