REGIOSELECTIVE LIPASE-MEDIATED ACYLATION-DEACYLATION IN THIADIAZINE DIACYCLONUCLEOSIDES
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 |