REGIOSELECTIVE LIPASE-MEDIATED ACYLATION-DEACYLATION IN THIADIAZINE DIACYCLONUCLEOSIDES

ESTEBAN, AI; JUANES, O; MARTINEZ, A; CONDE, S

Abstract

The first thiadiazine acyclonucleosides has been prepared, and so acyclic glycosylation of the SO2 analog of 6-methyluracil has been achieved. Regioselective deprotection of thiadiazine diacyclonucleoside has been performed by a combined strategy of enzyme-catalyzed hydrolysis-acylation.

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Título según WOS: ID WOS:A1994PU27900024 Not found in local WOS DB
Título de la Revista: TETRAHEDRON
Volumen: 50
Número: 48
Editorial: PERGAMON-ELSEVIER SCIENCE LTD
Fecha de publicación: 1994
Página de inicio: 13865
Página final: 13870
DOI:

10.1016/S0040-4020(01)85694-5

Notas: ISI