Zur Darstellung von 21‐Estern des Pregnen‐(5)‐diol‐(3β.21)‐ons‐(20) aus Pregnen‐(5)‐ol‐(3 β)‐on‐(20)
Author:
Affiliation:
1. Pharmazeutisch‐Wissenschaftlichen Laboratorien der Farbwerke Hoechst AG. vormals Meister Lucius & Brüning
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19550880618
Reference20 articles.
1. L. F.Fieseru.M.Fieser Chem. Techn.S.387.
2. Schering A. G. H. H.Inhoffen Dtsch. Bundes‐Pat.‐Anm. Sch. 3401/12 v. 13. 1. 1939/3. 7.1952.
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1. Hormones;Ullmann's Encyclopedia of Industrial Chemistry;2000-06-15
2. Syntheses of cis-dichlorodiammineplatinum analogs having steroidal hormones bound to the metal atom via malonato bridges;Inorganica Chimica Acta;1989-07
3. Preparation of radiolabeled pregnenolone analogs. 21-Fluoro- pregnenolone-21- 18F, 21-fluoropregnenolone-3-acetate-21- 18F, 21-fluoropregnenolone-7- 3H, and 21-fluoropregnenolone-3-acetate-7- 3H;Journal of Labelled Compounds and Radiopharmaceuticals;1983-01
4. Prostaglandins and congeners. 28. Synthesis of 2-(.omega.-carbalkoxyalkyl)cyclopent-2-en-1-ones, intermediates for prostaglandin syntheses;The Journal of Organic Chemistry;1980-11
5. BC → ABC → ABCD;Organic Chemistry: A Series of Monographs;1974
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