Epimerization at a quaternary C-substituted carbon atom
- 1 January 1981
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 37, 257-261
- https://doi.org/10.1016/0040-4020(81)85062-4
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- An improved synthesis of 13-epi-steroidsJournal of the Chemical Society, Chemical Communications, 1975
- Inversions of both adjacent centers in the formolysis of a 2,2,6-trialkylcyclohexyl tosylate. Formation of a 13.alpha.-D-homo steroidThe Journal of Organic Chemistry, 1973
- Hyperacidic media. A novel route to 13α-steroidsJournal of the Chemical Society, Chemical Communications, 1973
- Unexpected inversion of configuration at a quaternary centre during the acetolysis ofD-homo-5α-androstan-17aβ-yl tosylateJournal of the Chemical Society, Chemical Communications, 1973
- Epimerization about unactivated tertiary carbon atoms in substituted cyclopentane derivativesJournal of the American Chemical Society, 1968
- On the Mechanism of the Oxidative Cleavage of Phenyl-t-butylcarbinol with Chromic AcidJournal of the American Chemical Society, 1963
- Investigations on sterols XI : Preparation of 13α‐androstene derivativesRecueil des Travaux Chimiques des Pays-Bas, 1958
- The Mechanism of the Cleavage of Phenyl-t-butylcarbinol by Chromic AcidJournal of the American Chemical Society, 1956
- The Total Synthesis of Estrone and Three Stereoisomers Including LumiestroneJournal of the American Chemical Society, 1952
- Über Lumi‐oestronBerichte der deutschen chemischen Gesellschaft (A and B Series), 1941