Chemoselectivity in the conjugate addition of allylsilane to Michael acceptors
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (18) , 1909-1912
- https://doi.org/10.1016/s0040-4039(00)81803-1
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Reactions of allylsilanes and application to organic synthesisPublished by Walter de Gruyter GmbH ,1982
- Chemistry of organosilicon compounds 113 chemoselective allylation of carbonyl compounds with allylsilanes promoted by tetra--butylammonium fluoride. A new synthesis of homoallyl alcoholsTetrahedron Letters, 1978
- Use of dipolar aprotic solvents to alter the chemoselectivity of lithium dimethylcuprateThe Journal of Organic Chemistry, 1978
- Allylsilanes in organic synthesis: A facile intramolecular allyl transfer, evidence for a non-concerted processTetrahedron Letters, 1978
- Chemistry of organosilicon compounds. 99. Conjugate addition of allylsilanes to .alpha.,.beta.-enones. A New method of stereoselective introduction of the angular allyl group in fused cyclic .alpha.,.beta.-enonesJournal of the American Chemical Society, 1977
- Action d'organocuprates derivant de lithiens allyliques sur quelques derives carbonyles α-ethyleniques.Tetrahedron Letters, 1973
- Conjugate addition reactions with lithium diallylcuprateThe Journal of Organic Chemistry, 1969
- Reaction of lithium dialkyl- and diarylcuprates with organic halidesJournal of the American Chemical Society, 1969