Synthesis of 5 `-seleno-xylofuranosides


Autoria(s): BRAGA, Hugo C.; STEFANI, Helio A.; PAIXAO, Marcio W.; SANTOS, Francielli W.; LUEDTKE, Diogo S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

The synthesis of selenium derivatives of naturally occurring chiral molecules is becoming increasingly important in recent years. In this context, we describe herein an easy, straightforward synthetic route for the preparation of a series of chiral seleno-furanosides, starting from the readily available carbohydrate D-xylose. In addition, selected compounds were screened as inhibitors of the delta-aminolevulinate dehyclratase (delta-ALA-D) enzyme. Diselenide 4 was found to reduce significantly the enzymatic activity, while seleno-furanoside la increased delta-ALA-D activity. (C) 2010 Elsevier Ltd. All rights reserved.

FAPESP[07/02382-7]

CNPq[472064/2008-8]

Identificador

TETRAHEDRON, v.66, n.19, p.3441-3446, 2010

0040-4020

http://producao.usp.br/handle/BDPI/19666

10.1016/j.tet.2010.03.033

http://dx.doi.org/10.1016/j.tet.2010.03.033

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Tetrahedron

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #DELTA-AMINOLEVULINATE DEHYDRATASE #ASYMMETRIC ALLYLIC ALKYLATION #STEREOSELECTIVE-SYNTHESIS #OLIGOSACCHARIDE SYNTHESIS #CONTAINING OXAZOLINES #DIPHENYL DISELENIDE #EFFICIENT SYNTHESIS #D-XYLOSE #SELENIUM #SELENOGLYCOSIDES #Chemistry, Organic
Tipo

article

original article

publishedVersion