3α‐Acetoxy‐ätien‐(8:9 oder 8:14)‐säure‐methylester. Vorläufige Mitt. Über Gallensäuren und verwandte Stoffe 48. Mitteilung
- 1 January 1956
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 39 (6), 1507-1525
- https://doi.org/10.1002/hlca.19560390609
Abstract
Die Synthese von 3 α‐Acetoxy‐ätien‐(8:9 oder 8:14)‐säuremethylester wird beschrieben. Die Neubarechnung des molekularen Drehungsbeitrags fär die 8:14‐Doppelbindung in 5 β‐Steroiden ergibt einen Wert von etwa +70°.This publication has 47 references indexed in Scilit:
- THE SYNTHESIS OF LANOSTENOLJournal of the American Chemical Society, 1954
- Δ8,14-Cholestadiene-3β-yl-7-one AcetateJournal of the American Chemical Society, 1953
- The Dehydration of a Steroidal Δ8-11α-Hydroxy-7-ketoneJournal of the American Chemical Society, 1953
- Synthesis of 11-Ketosteroids.1 I. Dichromate Oxidation of a Bile Acid Δ7,9(11)-DieneJournal of the American Chemical Society, 1953
- Some Steroid MercaptolsJournal of the American Chemical Society, 1947
- Dehydration of Cholic AcidJournal of the American Chemical Society, 1946
- Hydrogenolysis of Sulfur Compounds by Raney Nickel CatalystJournal of the American Chemical Society, 1943
- The Preparation of the Homologs of 3-Hydroxy-12-ketocholanic AcidJournal of the American Chemical Society, 1943
- The Preparation of ▵8-, ▵8(14)- and ▵14-Cholestenes1Journal of the American Chemical Society, 1941
- Sterols. XVI. Lanosterol and AgnosterolJournal of the American Chemical Society, 1937