Regioselective reduction of benzylidene acetals from a bis-heterocyclic pyrimidino-pyranoside platform

After the preparation with few steps of the original bicyclic osidic scaffold of pyrimidino-pyranoside type, the exploration of the reactivity of the pyranose part allowed us to carry out different procedures for opening 4,6-O-benzylidene.

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Bibliographic Details
Published in:Mediterranean journal of chemistry 2021-09, Vol.11 (3), p.239
Main Authors: SAMB, Issa, Gaye, Mohamed Lamine
Format: Article
Language:English
Online Access:Get full text
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Summary:After the preparation with few steps of the original bicyclic osidic scaffold of pyrimidino-pyranoside type, the exploration of the reactivity of the pyranose part allowed us to carry out different procedures for opening 4,6-O-benzylidene.
ISSN:2028-3997
2028-3997
DOI:10.13171/mjc02109271584samb