DSpace at EWHA: Synthesis and biological evaluation of novel D-2′-azido-2′,3′-dideoxyarabinofuranosyl-4′- thiopyrimidines and purines

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DC Field	Value	Language
dc.contributor.author	정낙신	-
dc.date.accessioned	2016-08-28T11:08:03Z	-
dc.date.available	2016-08-28T11:08:03Z	-
dc.date.issued	2002	-
dc.identifier.issn	0960-894X	-
dc.identifier.other	OAK-1156	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/219041	-
dc.description.abstract	Novel D-2′-azido-2′,3′-dideoxyarabinofuranosyl-4′- thiopyrimidines and purines have been synthesized, starting from L-xylose via azidation at the 2′-position as a key step. Most of the final nucleosides exhibited toxicity-dependent anti-HIV-1 activity, among which D-α-adenine analogue 3h was found to be the most cytotoxic. © 2002 Elsevier Science Ltd. All rights reserved.	-
dc.language	English	-
dc.title	Synthesis and biological evaluation of novel D-2′-azido-2′,3′-dideoxyarabinofuranosyl-4′- thiopyrimidines and purines	-
dc.type	Article	-
dc.relation.issue	17	-
dc.relation.volume	12	-
dc.relation.index	SCI	-
dc.relation.index	SCIE	-
dc.relation.index	SCOPUS	-
dc.relation.startpage	2403	-
dc.relation.lastpage	2406	-
dc.relation.journaltitle	Bioorganic and Medicinal Chemistry Letters	-
dc.identifier.doi	10.1016/S0960-894X(02)00394-3	-
dc.identifier.wosid	WOS:000177603200032	-
dc.identifier.scopusid	2-s2.0-1842853496	-
dc.author.google	Kim H.O.	-
dc.author.google	Park Y.H.	-
dc.author.google	Moon H.R.	-
dc.author.google	Jeong L.S.	-
dc.contributor.scopusid	정낙신(16028528200)	-
dc.date.modifydate	20211210153610	-