Issue 22, 1969

Enzymic formation of a tricyclic sesterterpene alcohol from mevalonic acid and all-trans-geranylfarnesyl pyrophosphate

Abstract

Mevalonic acid lactone and the chemically synthesized all-trans-geranylfarnesyl pyrophosphate are converted into a tricyclic sesterterpene alcohol, ophiobolin F, by incubation with 100,000 ×g supernatant fraction from cell-free system of Chochlibolus heterostrophus.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 1319-1320

Enzymic formation of a tricyclic sesterterpene alcohol from mevalonic acid and all-trans-geranylfarnesyl pyrophosphate

S. Nozoe and M. Morisaki, J. Chem. Soc. D, 1969, 1319 DOI: 10.1039/C29690001319

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