New short route to unsaturated fluoroketonucleosides: Case of 5-fluoro-1-(6-O-acetyl-3,4-di-deoxy-3-fluoro-beta-D-glycero-hex-3-eno-py ranos-2-ulosyl) uracil

dc.creator	Egron, M. J.	en
dc.creator	Komiotis, D.	en
dc.creator	Dorange, I.	en
dc.creator	Herscovici, J.	en
dc.creator	Ollapally, A. P.	en
dc.creator	Antonakis, K.	en
dc.date.accessioned	2015-11-23T10:26:05Z
dc.date.available	2015-11-23T10:26:05Z
dc.date.issued	2005
dc.identifier	10.1081/ncn-200059683
dc.identifier.issn	1525-7770
dc.identifier.uri	http://hdl.handle.net/11615/27294
dc.description.abstract	The proposed short synthesis involves two key steps: Oxidation of the isopropylidene derivative of the 3 fluoronucleoside possessing a free hydroxyl group in 2-position and acetylation of deprotected 3-fluoro-2-ketonucleoside which, after a beta-elimination reaction, gives the desired unsaturated ketonucleoside 5.	en
dc.source.uri	<Go to ISI>://WOS:000230392700002
dc.subject	BIOLOGICAL-ACTIVITY	en
dc.subject	DERIVATIVES	en
dc.subject	AGENT	en
dc.subject	Biochemistry & Molecular Biology	en
dc.title	New short route to unsaturated fluoroketonucleosides: Case of 5-fluoro-1-(6-O-acetyl-3,4-di-deoxy-3-fluoro-beta-D-glycero-hex-3-eno-py ranos-2-ulosyl) uracil	en
dc.type	journalArticle	en

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