Issue 6, 1992
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Regioselective enzymatic acetylation of methyl 4,6-O-benzylidene-α- and β-D-glucopyranoside

Matthew J. Chinn,   Gilles Lacazio,   David G. Spackman,   Nicholas J. Turner  and  Stanley M. Roberts  

Abstract

Lipase-catalysed acetylation of 1 furnishes the ester 3 in 94% yield while, under the same reaction conditions, the isomer 2 affords the ester 5 in 86% yield.

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Article information

DOI
https://doi.org/10.1039/P19920000661
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 661-662

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Regioselective enzymatic acetylation of methyl 4,6-O-benzylidene-α- and β-D-glucopyranoside

M. J. Chinn, G. Lacazio, D. G. Spackman, N. J. Turner and S. M. Roberts, J. Chem. Soc., Perkin Trans. 1, 1992, 661 DOI: 10.1039/P19920000661

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