Microbiological transformations. Part 5. Microbiological transformations of 17a-aza- and 17-aza-D-homoandrost-5-ene derivatives with the fungus Cunninghamella elegans
- 1 January 1982
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 2,p. 571-576
- https://doi.org/10.1039/p19820000571
Abstract
The products obtained from the incubation of 17a-aza- and 17-aza-D-homoandrost-5-ene derivatives with Cunninghamella elegans are largely those resulting from allylic oxidation or epoxidation of the Δ5-bond. The substrates are predominantly monohydroxylated whereas androst-5-ene derivatives under the same conditions show a tendency towards dihydroxylation.This publication has 0 references indexed in Scilit: