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

DOI: 10.1016/S0022-328X(00)87068-0

Source and publish data:

Journal of Organometallic Chemistry p. 139 - 148 (1982)

Update date:2022-07-30

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Authors:

Doucoure, A.

Mauze, B.

Miginiac, L.

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Article abstract of DOI:10.1016/S0022-328X(00)87068-0

Chloroallyllithium readily reacts with aliphatic and aromatic aldehydes and ketones to produce, in a one-step reaction, Z-γ-chlorinated-β-ethylenic alcohols and bi- or tri-substituted epoxides.

Full text of DOI:10.1016/S0022-328X(00)87068-0

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