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HERO ID
7744030
Reference Type
Journal Article
Title
Enantioselective acylation of 2-hydroxymethyl-2,3-dihydrobenzofurans catalysed by lipase from Pseudomonas cepacia (Amano PS) and total stereoselective synthesis of (-)-(R)-MEM-protected arthrographol
Author(s)
Ramadas, S; Krupadanam, GLD
Year
2000
Is Peer Reviewed?
1
Journal
Tetrahedron: Asymmetry
ISSN:
0957-4166
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Location
OXFORD
Volume
11
Issue
16
Page Numbers
3375-3393
Language
English
DOI
10.1016/S0957-4166(00)00302-5
Web of Science Id
WOS:000089843700017
Abstract
Lipase Amano PS catalysed acylation of (±)-2-hydroxymethyl-2,3-dihydrobenzofurans using vinyl acetate as the acyl donor in n-hexane gave (-)-(R)-2-acetoxymethyl-2,3-dihydrobenzofurans and (+)-(S)-2-hydroxymethyl-2,3-dihydrobenzofurans in high enantiomeric excess. (-)-(R)-Acetate 18j is converted to (-)-(R)-MEM-protected arthrographol 22. Copyright (C) 2000 Elsevier Science Ltd.
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