Additivity relationships in carbon-13 nuclear magnetic resonance spectra of dihydroxy steroids.
Explore the source record for details and available documents.
Hydroxysteroids↗
Biomedical subjects
G D Meakins
Publications and source records attributed to G D Meakins.
Microbiological hydroxylation. Part XXII. Hydroxylation of 3,20-, 7,20-, and 11,20-dioxygenated 5alpha-pregnanes.
Explore the source record for details and available documents.
Hydroxylation↗
Preparation of 3beta-hydroxy-5alpha-androstan-16-one.
Explore the source record for details and available documents.
Dihydrotestosterone↗
Microbiological hydroxylation. Part XVII. Introduction of 16alpha-, 9alpha-, and 3alpha-hydroxy-groups into dioxygenated 5alpha-androstanes by the fungus Diaporthe celastrina.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation. Part XVI. Incubation of derivatives (mainly acetals) of 5alpha-androstane ketones with the fungi Calonectria decora, Aspergillus ochraceus, and Rhizopus nigricans.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation. Part XIX. The action of an ant fungus ('Acromyrmex fungus') on oxygenated androstanes, pregnanes, and cholestanes.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation. Part XX. Hydroxylation of dioxygenated 5alpha-androstanes with the fungi Absidia regnieri and Syncephelastrum racemosum.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation. Part XXI. Hydroxylations of 3-halogeno-17-oxo-, 3-halogeno-7-oxo-, and 17-halogeno-3-oxo-androstanes by the fungi Calonectria decora, Rhizopus nigricans, and Aspergillus ochraceus.
Explore the source record for details and available documents.
17-Ketosteroids↗
Microbiological hydroxylation. XIV. Hydroxylation in the terminal rings of dioxygenated 5alpha-androstanes with the fungi Wojnowicia graminis and Ophiobolus herpotrichus.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation. XV, Hydroxylation in the terminal rings of mono- and di-oxygenated 5alpha-androstanes with the fungus Daedalea rufescens.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation. Part XVII. C-19 hydroxylation of 17-oxo-5alpha-androstanes and 17-oxo-3alpha, 5-cyclo-5alpha-androstanes by the fungus Calonectria decora.
Explore the source record for details and available documents.
17-Ketosteroids↗
Microbiological hydroxylation of steroids. XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5 alpha-androstanes and to 5 alpha-androstan-11-one.
Explore the source record for details and available documents.
Androstanes↗
Studies in the steroid group. (part)LXXXXV. Convenient preparations of 3,6- and 6,17-dioxygenated 5alpha-androstanes.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation of steroids. VII. The pattern of dihydroxylation of mono-oxo-5 alpha-androstanes and 5 alpha-estranes with the fungus Rhizopus nigricans.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation of steroids. 8. The pattern of monohydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with cultures of the fungus, Rhizopus nigricans.
Explore the source record for details and available documents.
Alcohols↗
Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signals.
Explore the source record for details and available documents.
Androstanes↗
Microbiological hydroxylation of steroids. X. 1 beta, 11 alpha-dihydroxylation of 3 beta-hydroxy-5 alpha-prepnan-20-one and the hydroxylation of other 20-oxo-5 alpha-pregnanes with the fungus Aspergillys ochraceus.
Explore the source record for details and available documents.
Aspergillus↗
Studies in in the steroid group. LXXXII. The preparation of nine mono- and eight di-oxoandrostanes, 5 -estran-17-one, and 5 -pregnane-2,20-dione.
Explore the source record for details and available documents.
Androstanes↗