Enantioselective synthesis of ring-C aromatic steroids by asymmetric Michael-type alkylation of chiral imines.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (21) , 2367-2370
- https://doi.org/10.1016/s0040-4039(00)96126-4
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Toward a transition-state model in the asymmetric alkylation of chiral ketone secondary enamines by electron-deficient alkenes. A theoretical MO studyThe Journal of Organic Chemistry, 1986
- Bruceantin support studies. 10. Use of an axial .alpha.-face control element in intramolecular conjugate additions: synthesis of an ABCD tetracyclic bruceantin precursorThe Journal of Organic Chemistry, 1986
- Enantioselective synthesis of quaternary carbon centers through Michael-type alkylation of chiral iminesJournal of the American Chemical Society, 1985
- Total synthesis of ring-c aromatic 18-nor steroidTetrahedron, 1980
- Synthesis of ring-C aromatic steroidsThe Journal of Organic Chemistry, 1979
- Stereoselective total syntheses of diterpene resin acidsThe Journal of Organic Chemistry, 1977
- Stereochemical studies. XLII. Asymmetric synthesis of naturally occurring podocarpic acid.CHEMICAL & PHARMACEUTICAL BULLETIN, 1976
- Stereochemical studies. XLI. Asymmetric synthesis of optically active 4a-methyl-4,4a,9,10-tetrahydro-2(3H)-phenanthrone derivatives, key intermediates for total syntheses of optically active diterpenes and steroids.CHEMICAL & PHARMACEUTICAL BULLETIN, 1976