Issue 2, 1991

Enantiospecific synthesis of (4S,5S,6S)-4,5,6-trihydroxycyclohex-2-enone and (+)-conduritol C from fluorobenzene via microbial oxidation

Abstract

Epoxidation of the chiral diene 5, produced by Pseudomonas putida oxidation of fluorobenzene, gave fluoroconduritol 9 and cyclohexenone 11; the latter was used in a short synthesis of (+)-conduritol C 1.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 61-62

Enantiospecific synthesis of (4S,5S,6S)-4,5,6-trihydroxycyclohex-2-enone and (+)-conduritol C from fluorobenzene via microbial oxidation

H. A. J. Carless and O. Z. Oak, J. Chem. Soc., Chem. Commun., 1991, 61 DOI: 10.1039/C39910000061

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