Issue 11, 1981
From the journal:

Journal of the Chemical Society, Chemical Communications

Detection of one symmetrical precursor during the biosynthesis of the fungal metabolite austdiol using [1,2-13C2]acetate and [Me-13C]methionine

Lino Colombo,   Cesare Gennari,   Giuliana Severini Ricca,   Carlo Scolastico  and  Fabrizio Aragozzini  

Abstract

A13C n.m.r. analysis of [1,2-13C2]acetate- and [Me–13C]methionine-derived austdiol (1) is consistent with the symmetrical aldehyde (2) being a biosynthetic precursor of (1).

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Article information

DOI
https://doi.org/10.1039/C39810000575
Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 575-576

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Detection of one symmetrical precursor during the biosynthesis of the fungal metabolite austdiol using [1,2-13C2]acetate and [Me-13C]methionine

L. Colombo, C. Gennari, G. S. Ricca, C. Scolastico and F. Aragozzini, J. Chem. Soc., Chem. Commun., 1981, 575 DOI: 10.1039/C39810000575

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