A 13C 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).
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.M.A. Gennari, G. S. Ricca, C. Scolastico, F. Aragozzini. - In: JOURNAL OF THE CHEMICAL SOCIETY, CHEMICAL COMMUNICATIONS. - ISSN 0022-4936. - 11(1981), pp. 575-576. [10.1039/C39810000575]
Detection of one symmetrical precursor during the biosynthesis of the fungal metabolite austdiol using [1,2-13C2]acetate and [Me-13C]methionine
C.M.A. Gennari;C. Scolastico;
1981
Abstract
A 13C 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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