Simple regioselective synthesis of trans-7a-methylhydrind-4-en-1-one, a key intermediate for steroid total synthesis
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (40) , 3929-3932
- https://doi.org/10.1016/s0040-4039(01)82029-3
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- New stereoselective synthesis of steroidsJournal of the American Chemical Society, 1981
- Silicon in synthesis: an exceptionally short synthesis of dl-11.alpha.-hydroxyestrone methyl etherJournal of the American Chemical Society, 1980
- Synthesis of (.+-.)-coronafacic acid. Efficient intramolecular Diels-Alder reaction of latent diene-dienophile functionality via thermal reactionJournal of the American Chemical Society, 1980
- An efficient and versatile generation of o-xylylenes by fluoride anion induced 1,4 elimination of o-(.alpha.-trimethylsilylalkyl)benzyltrimethylammonium halidesJournal of the American Chemical Society, 1980
- Thermal, photochemical, and transition-metal mediated routes to steroids by intramolecular Diels–Alder reactions of o-xylylenes (o-quinodimethanes)Chemical Society Reviews, 1980
- Control elements in the intramolecular Diels-Alder reaction. Synthesis of (.+-.)-torreyolJournal of the American Chemical Society, 1979
- Stereospecific total synthesis of (.+-.)-warburganal and related compoundsJournal of the American Chemical Society, 1979
- Δ5-octahydro-1-naphtalenones and Δ5-decahydro-1-naphthalenes (-1-decalones) by stereoselective intramolecular diels-alder reaction.Tetrahedron Letters, 1979
- Intramolecular alkylation of internal chloro olefins. Facile route to the D ring in 20-keto steroidsJournal of the American Chemical Society, 1971