SE' Addition of homochiral α-alkoxyallylstannanes to aldehydes
- 1 January 1989
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 45 (4) , 1043-1052
- https://doi.org/10.1016/0040-4020(89)80015-8
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Cembranolide total synthesis. Macrocyclization of (.alpha.-alkoxyallyl)stannane-acetylenic aldehydes as a route to cembrane lactonesThe Journal of Organic Chemistry, 1988
- Synthesis of homochiral α-alkoxystannanes: stereospecific conversion to cembranolide precursorsTetrahedron Letters, 1988
- Acyclic stereocontrol via allylic organometallic compoundsAccounts of Chemical Research, 1987
- Asymmetric synthesis via axially dissymmetric molecules. 7. Synthetic applications of the enantioselective reduction by binaphthol-modified lithium aluminum hydride reagentsJournal of the American Chemical Society, 1984
- Asymmetric synthesis via axially dissymmetric molecules. 6. Rational designing of efficient chiral reducing agents. Highly enantioselective reduction of aromatic ketones by binaphthol-modified lithium aluminum hydride reagentsJournal of the American Chemical Society, 1984
- Stereo- and regiocontrol of acyclic systems via the lewis acid mediated reaction of allylic stannanes with aldehydesTetrahedron, 1984
- Observations on the choice of Lewis acid and mode of addition for the Lewis acid mediated reaction of crotyltri- -butylstannane with aldehydes: convenient and highly selective access to both and productsTetrahedron Letters, 1984
- .alpha.-Alkoxyorganolithium reagents. A new class of configurationally stable carbanions for organic synthesisJournal of the American Chemical Society, 1980
- Stannylation/destannylation. Preparation of .alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalentJournal of the American Chemical Society, 1978
- Efficient Methods for Oxidation of AlcoholsBulletin of the Chemical Society of Japan, 1977