Issue 14, 1992

Enzyme-catalysed hydrolysis of 3,5-cis-diacetoxy-4-trans-benzyloxy-methylcyclopentene and the synthesis of aristeromycin precursors

Abstract

The optically active mono-ester 2 was obtained by enzyme-catalysed hydrolysis of the diester 1 and converted into the azide 8 and the amine 13, synthetic precursors of (+)- and (–)-aristeromycin.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 1751-1752

Enzyme-catalysed hydrolysis of 3,5-cis-diacetoxy-4-trans-benzyloxy-methylcyclopentene and the synthesis of aristeromycin precursors

D. M. LeGrand and S. M. Roberts, J. Chem. Soc., Perkin Trans. 1, 1992, 1751 DOI: 10.1039/P19920001751

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