Asymmetric Michael-type alkylation of chiral imines. Enantioselective syntheses of (−)-geosmin and two other related natural terpenes, as well as enant-(+)-geosmin
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (31) , 4121-4124
- https://doi.org/10.1016/s0040-4039(00)99338-9
Abstract
No abstract availableThis publication has 23 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
- Enantioselective preparation of key [ABC] intermediates for steroid synthesis through the asymmetric Michael addition process involving chiral imines.Tetrahedron Letters, 1988
- Enantioselective synthesis of ring-C aromatic steroids by asymmetric Michael-type alkylation of chiral imines.Tetrahedron Letters, 1987
- Musty/earthy aromasFood Reviews International, 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
- Geosmin, from microorganisms, is -1, 10-dimethyl--9-decalolTetrahedron Letters, 1968
- Synthesis of (+-)-geosmin and the other 1,10-dimethyl-9-decalol isomersThe Journal of Organic Chemistry, 1968
- Oxygenation of 1,10-Dimethyl-1(9)-octalinThe Journal of Organic Chemistry, 1966