New bis- and tris-annulation reagents for the syntheses of CD rings of steroids, bearing a functionalized 18-methyl group, by the palladium-catalyzed cyclization
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (35), 3393-3394
- https://doi.org/10.1016/s0040-4039(00)78697-7
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Preparation of five- and six- membered cyclic ketones by the palladium-catalyzed cyclization reaction. Application to methyl dihydrojasmonate synthesisTetrahedron Letters, 1980
- A new bisannulation reagent easily prepared from a butadiene telomer, and its application to steroid synthesisJournal of the American Chemical Society, 1979
- Investigations on Steroids. XIII. Synthesis of the Compounds related to the Metabolites of Furazabol (17β-Hydroxy-17α-methyl-5α-androstano [2, 3-c] furazan)CHEMICAL & PHARMACEUTICAL BULLETIN, 1972
- A Stereospecific Total Synthesis of 18-Substituted Steroids. Application to the Synthesis of dl-ConessineJournal of the American Chemical Society, 1962
- Total Synthesis of Racemic ConessineJournal of the American Chemical Society, 1962
- THE SYNTHESIS OF DIHYDROCONESSINE. A METHOD FOR FUNCTIONALIZING STEROIDS AT C18Journal of the American Chemical Society, 1958