Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/94852
Type: Artigo de periódico
Title: Stereoselective Synthesis Of Azanucleosides Aza-stavudine (aza-d4t), Aza-2′,3′-didehydro-3′-deoxyuridine (aza-d4u), And Its Hydrogenated Analogues From An Endocyclic Enecarbamate
Author: Costenaro E.R.
Fontoura L.A.M.
Oliveira D.F.
Correia C.R.D.
Abstract: The stereoselective synthesis of the aza-analogues of nucleosides stavudine (D4T) and dideoxyuridine (DDU) were accomplished in a very concise manner (3-4 step sequences) with high overall yields from a five-membered endocyclic enecarbamate employing phenylselenenyl bromide as an effective promoter. © 2001 Elsevier Science Ltd.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/S0040-4039(00)02343-1
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0035951975&partnerID=40&md5=568e2bc03ef6925058a53cca7345a6d0
Date Issue: 2001
Appears in Collections:Unicamp - Artigos e Outros Documentos

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