The asymmetric michael process involving chiral imines: The diastereofacial differentiation aspect
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (20), 2645-2648
- https://doi.org/10.1016/s0040-4039(00)99088-9
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Enantioselective synthesis of oxa-spiro compoundsTetrahedron Letters, 1989
- The asymmetric michael addition process involving chiral imines : stereochemical data in support of a cyclic-like transition stateTetrahedron Letters, 1988
- Conformational model for asymmetric Diels-Alder reactions with chiral dienesTetrahedron Letters, 1988
- Enantioselective preparation of key [ABC] intermediates for steroid synthesis through the asymmetric Michael addition process involving chiral imines.Tetrahedron Letters, 1988
- The preparation of optically active δ2- isoxazolines. A model for asymmetric induction in the non lewis acid catalyzed reactions of oppolzer's chiral sultamTetrahedron Letters, 1988
- Stable and reactive conformations of N-enoyl-bornane-10.2-sultams in the absence of lewis acids : asymmetric 1.4-hydride additionsTetrahedron Letters, 1988
- Enantioselective synthesis of ring-C aromatic steroids by asymmetric Michael-type alkylation of chiral imines.Tetrahedron Letters, 1987
- 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
- Enantioselective synthesis of quaternary carbon centers through Michael-type alkylation of chiral iminesJournal of the American Chemical Society, 1985
- Structural Studies of Crystalline EnaminesHelvetica Chimica Acta, 1978