Total synthesis in the steroid series. I. An tricyclic intermediate to 18‐oxygenated steroids. d,l‐Δ8a‐4bβ‐Methyl‐2β‐formyl‐2α‐(3′‐oxopropyl)‐7‐ethylenedioxy‐4aα,10aβ‐dodecahydrophenanthrene‐4β‐ol‐l‐one)
- 1 January 1956
- journal article
- research article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 75 (9) , 1043-1052
- https://doi.org/10.1002/recl.19560750906
Abstract
The total synthesis of racemic aldosterone (I) was achieved recently by J. Schmidlin, G. Anner, J.‐R. Billeter and A. Wettstein A. Wettstein at the XIVth International Congres of Pure and Applied Chemistry, July 1955, Zürich. Experientia 11, 365 (1955). . Our own efforts in the field of the total synthesis of adrenal cortical hormones and derivatives will be described in the present and forthcoming papers See Experientia 11, 365 (1955), footnote 2.Keywords
This publication has 4 references indexed in Scilit:
- Die Konstitution des Aldosterons. Über Bestandteile der Nebennierenrinde und verwandte Stoffe. 92. MitteilungHelvetica Chimica Acta, 1954
- Conjugation and the Intensity of the Infrared Carbonyl BandThe Journal of Chemical Physics, 1953
- Approaches to the Total Synthesis of Adrenal Steroids. VI. 2,4b-Dimethyl-7-ethylenedioxy-1,2,3,4,4aα,4b,5,6,7,8,10,10aβ- dodecahydrophenanthrene-4β-ol-1-one and Related CompoundsJournal of the American Chemical Society, 1953
- Approaches to the Total Synthesis of Adrenal Steroids.1 V. 4b-Methyl-7- ethylenedioxy-1,2,3,4,4aα,4b,5,6,7,8,10,10a β-dodecahydrophenanthrene-4 β-ol-1-one and Related Tricyclic DerivativesJournal of the American Chemical Society, 1953