Reaction du gem-chloro(methyl)allyllithium sur les aldehydes et les cetones: nouvelle methode de synthese d'epoxydes α-ethyleniques tri-et tetra-substitues
- 8 May 1979
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 170 (3) , 265-270
- https://doi.org/10.1016/s0022-328x(00)92064-3
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Diethyl 1-Chloro-1-lithioalkanephosphonates. A General Synthesis of Diethyl 1,2-Epoxyalkanephosphonates and 1-Alkoxycarbonyl-1-chloroalkanephosphonatesSynthesis, 1978
- Reaction of gem-dichloroallyllithium with aldehydes, ketones, and other organic substrates. An example of electronic control of regioselectivity in the reactions of an ambident nucleophileJournal of the American Chemical Society, 1977
- The Magnesium Derivative of Thioacrolein Dianion. A Facile Entry to Vinyl‐ and DivinyloxiranesAngewandte Chemie International Edition in English, 1976
- Regiospecific synthesis of αβ-unsaturated epoxidesTetrahedron Letters, 1976
- gem-Dichloroallyllithium: A seemingly ambident nucleophileJournal of Organometallic Chemistry, 1974