Issue 10, 1991

Enzymatic resolution of cis- and trans-4-hydroxycyclopent-2-enylmethanol derivatives and a novel preparation of carbocyclic 2′,3′-dideoxydidehydronucleosides and aristeromycin

Abstract

The (1R, 4S)-acetate 3 and the (1S, 4S)-alcohol 5 have been obtained optically pure by lipase catalysed esterification: compounds 3 and 5 have been converted into carbocyclic dideoxydidehydronucleosides and aristeromycin 9.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 2605-2607

Enzymatic resolution of cis- and trans-4-hydroxycyclopent-2-enylmethanol derivatives and a novel preparation of carbocyclic 2′,3′-dideoxydidehydronucleosides and aristeromycin

S. M. Roberts and K. A. Shoberu, J. Chem. Soc., Perkin Trans. 1, 1991, 2605 DOI: 10.1039/P19910002605

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