Reaction du chloroallyllithium et du gem-chloro(methyl)allyllithium sur les esters: Nouvelle methode de synthese de cetones chlorees ethyleniques et d'acyloines ethyleniques-Reference-Cited by-同舟云学术

Reaction du chloroallyllithium et du gem-chloro(methyl)allyllithium sur les esters: Nouvelle methode de synthese de cetones chlorees ethyleniques et d'acyloines ethyleniques

Published:1981-07 Issue:1 Volume:215 Page:1-8
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:fr
Short-container-title:Journal of Organometallic Chemistry

Author:

Mauze B.,Doucoure A.,Miginiac L.

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference11 articles.

1. Reaction du gem-chloro(methyl)allyllithium sur les aldehydes et les cetones: nouvelle methode de synthese d'epoxydes α-ethyleniques tri-et tetra-substitues

2. Reaction du gem-chloro(methyl)allyllithium sur les aldimines et les cetimines: nouvelle methode de synthese d'aziridines α-ethyleniques N-substituees

3. gem-Dichloroallyllithium: A seemingly ambident nucleophile

4. Reaction of gem-dichloroallyllithium with aldehydes, ketones, and other organic substrates. An example of electronic control of regioselectivity in the reactions of an ambident nucleophile

5. gem-chloro(trimethylsilyl)allyllithium: A novel ambident nucleophile

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