Controllable regioselective enzymatic synthesis of polymerizable 5'-O-vinyl- and 3'-O-vinyl-nucleoside analogues in acetone.

Abstract:

:An efficient synthesis of polymerizable 3'- and 5'-O-acyl-nucleoside derivatives has been developed from inosine and 2'-deoxyuridine by enzyme-catalyzed regioselective acylation with divinyl dicarboxylates. In acetone, Lipozyme (immobilized lipase from Mucor miehei) gave 5'-O-acyl-nucleoside products, and PPL (lipase from porcine pancreas) provided 3'-O-acyl-nucleoside products.

journal_name

Biotechnol Lett

journal_title

Biotechnology letters

authors

Sun XF,Wang N,Wu Q,Lin XF

doi

10.1023/b:bile.0000030050.20353.a6

keywords:

subject

Has Abstract

pub_date

2004-06-01 00:00:00

pages

1019-22

issue

12

eissn

0141-5492

issn

1573-6776

pii

5278757

journal_volume

26

pub_type

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