Use of the carbopalladation of 1,2-propadiene in a two step synthesis of steroids
- 11 February 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (7) , 915-918
- https://doi.org/10.1016/s0040-4039(00)92119-1
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Enantioselective approach to the steroid skeleton by conjugate addition of alkenylcopper-phosphine complexes. Total syntheses of estrone methyl ether and its 7-alkylated derivativeTetrahedron Letters, 1990
- Syntheses and Reactions of 2-Alkyl-1,3-cyclopentanediones (2-Alkyl-3-hydroxy-2-cyclopenten-1-ones)Synthesis, 1989
- Vinyl trifluorosulfonates in the carbopalladation of allenic hydrocarbonsTetrahedron Letters, 1988
- Carbopalladation of allenic hydrocarbons.Tetrahedron, 1987
- Steroid total synthesisRecueil des Travaux Chimiques des Pays-Bas, 1986
- Stereoselectivity in intramolecular diels-alder reactions; a short total synthesis of (±)-estroneTetrahedron Letters, 1984
- Termination of biomimetic cyclizations by the allylsilane function. Formation of the steroid nucleus in one step from an acyclic polyenic chainJournal of the American Chemical Society, 1983
- Regioselective 1,4-addition of nucleophiles to 1,3-diene monoepoxides catalyzed by palladium complexTetrahedron Letters, 1981
- An enantiodirected cyclopentenone annulation. Synthesis of a useful building block for condensed cyclopentanoid natural productsJournal of the American Chemical Society, 1980
- Total synthesis of 11.beta.-methyl-19-norsteroidsThe Journal of Organic Chemistry, 1976