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Issue 0, 1980

Microbiological transformations. Part 3. The oxidation of androstene derivatives with the fungus Cunninghamella elegans

Abstract

The products obtained from the incubation of some Δ4- and Δ5-androstene derivatives with Cunninghamella elegans are largely those arising from allylic oxidation or epoxidation of the double bond, but some 9-, 12-, 14-, and 16-hydroxylation also occurs.

Article information


J. Chem. Soc., Perkin Trans. 1, 1980, 2535-2541
Article type
Paper

Microbiological transformations. Part 3. The oxidation of androstene derivatives with the fungus Cunninghamella elegans

T. A. Crabb, P. J. Dawson and R. O. Williams, J. Chem. Soc., Perkin Trans. 1, 1980, 2535 DOI: 10.1039/P19800002535

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