Eine einfache Methode zur Herstellung von in Ring A ungesättigten 9, 11-Dehydro-16α-methyl-steroiden. Über Steroide, 162. Mitteilung
- 1 January 1960
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 43 (2), 523-529
- https://doi.org/10.1002/hlca.19600430209
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Über 11,18‐dioxygenierte Progesterone. Über Steroide, 161. MitteilungHelvetica Chimica Acta, 1959
- Über 9,11-ungesättigte 16α-Methylallopregnene. Über Steroide 160. Mitt.Helvetica Chimica Acta, 1959
- Sterische Einflüsse einer 16α‐Methylgruppe auf Reaktionen in der Seitenkette von Allopregnan‐VerbindungenHelvetica Chimica Acta, 1959
- 16-ALKYLATED CORTICOIDS. II. 9α-FLUORO-16α-METHYLPREDNISOLONE 21-ACETATE1Journal of the American Chemical Society, 1958
- 16-METHYLATED STEROIDS. II. 16α-METHYL ANALOGS OF CORTISONE, A NEW GROUP OF ANTI-INFLAMMATORY STEROIDS. 9α-HALO DERIVATIVESJournal of the American Chemical Society, 1958
- Synthese von 18‐Carboxy‐steroiden. Über Steroide, 146. MitteilungHelvetica Chimica Acta, 1957
- Bromination of 5α,6β-Dibromocholestane-3-oneJournal of the American Chemical Society, 1955
- Steroids. IV.1a α-Iodoketones. A Method for the Conversion of Allosteroids into ▵4-3-Ketosteroids1bJournal of the American Chemical Society, 1950
- Studies in Steroid Metabolism. IX. Further Observations on the Infrared Absorption Spectra of Ketosteroids and Steroid EstersJournal of the American Chemical Society, 1950