Issue 23, 1972

Mechanism of alkylation during sitosterol biosynthesis in Larix decidua

Abstract

Incorporation of [2-14C-(4R)-4-3H1]mevalonic acid into sitosterol in Larix decidua demonstrates that during alkylation, the C-24 hydrogen of the Δ24 precursor is eliminated.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1295-1296

Mechanism of alkylation during sitosterol biosynthesis in Larix decidua

P. J. Randall, H. H. Rees and T. W. Goodwin, J. Chem. Soc., Chem. Commun., 1972, 1295 DOI: 10.1039/C39720001295

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