Chiral trans hydrindenones : synthesis of optically pure [3aαH(S), 7aβMe(S)trans-1-methyl-7a-methylhydrindan-1,4-diene-6-one
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (6) , 685-688
- https://doi.org/10.1016/s0040-4039(00)99972-6
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- A new route to functionalized trans-hydrindenonesJournal of the American Chemical Society, 1983
- Acid catalyzed intramolecular conjugate addition as a route to trans hydrindane systemsTetrahedron Letters, 1983
- New construction of a steroidal ring system. Stereoselective synthesis of (.+-.)-androstane-2,17-dioneThe Journal of Organic Chemistry, 1983
- Highly stereoselective claisen rearrangement of vinyl ether of 1-(1-hydroxyethyl)-2-methyl-3-alkylcyclopentene. A route to cis- and trans (1E)-ethylidene-8-methylhydrindan-5-one.Tetrahedron Letters, 1982
- A stereoselective approach to steroid trans-C/D ring synthonsThe Journal of Organic Chemistry, 1982
- Stereochemical control of intramolecular conjugate addition. A short, highly stereoselective synthesis of adrenosteroneJournal of the American Chemical Society, 1982
- New route to 11-oxygenated steroidsJournal of the American Chemical Society, 1981
- Bicyclo[2.2.1]heptanes in organic synthesis. Stereocontrolled approach to sterol side-chain construction: synthesis of De-AB-cholest-11-en-9-oneJournal of the American Chemical Society, 1979
- A stereocontrolled approach toward vitamin D metabolites. A synthesis of the Inhoffen-Lythgoe diolJournal of the American Chemical Society, 1979
- Asymmetric induction in 19-norsteroid total synthesisAccounts of Chemical Research, 1976