Le chloroallyllithium comme synthon de chloroallylation ou comme equivalent du vinylcarbene: Synthese regioselective d'alcools γ-ethyleniques β-chlores et de vinyl-2 oxetanes a partir d'epoxydes-Reference-Cited by-同舟云学术

Le chloroallyllithium comme synthon de chloroallylation ou comme equivalent du vinylcarbene: Synthese regioselective d'alcools γ-ethyleniques β-chlores et de vinyl-2 oxetanes a partir d'epoxydes

Published:1985-04 Issue:2 Volume:284 Page:139-147
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:fr
Short-container-title:Journal of Organometallic Chemistry

Author:

Ongoka P.,Mauzé B.,Miginiac L.

Publisher

Elsevier BV

Subject

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

Reference25 articles.

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

2. Action du chloroallyllithium sur les aldehydes et les cetones: synthese en une etape d'alcools β-ethyleniques γ-chlores de configuration z et d'epoxydes α-ethyleniques bi- ou tri-substitues

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

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

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