A highly efficient synthesis of (Z) γ-iodo allylic alcohols

Marek, Ilane; Alexakis, Alexandre; Normant, Jean-F.

doi:10.1016/S0040-4039(00)92377-3

Scientific article

Letter

English

A highly efficient synthesis of (Z) γ-iodo allylic alcohols

ContributorsMarek, Ilane; Alexakis, Alexandre; Normant, Jean-F.

Published inTetrahedron letters, vol. 32, no. 39, p. 5329-5332

Publication date1991

Abstract

The reaction of (Z) Methyl-ß-iodo propenoate with diisobutylaluminium hydride and subsequent reaction with a Grignard reagent allows the synthesis of (Z) ?-iodo allylic alcohols in a very easy way.

Keywords

ß-Halopropenoate
(Z) ?-iodo allylic alcohols
(Z) ?-iodo acrolein equivalent

Affiliation entities

Not a UNIGE publication

Citation (ISO format)

MAREK, Ilane, ALEXAKIS, Alexandre, NORMANT, Jean-F. A highly efficient synthesis of (Z) γ-iodo allylic alcohols. In: Tetrahedron letters, 1991, vol. 32, n° 39, p. 5329–5332. doi: 10.1016/S0040-4039(00)92377-3

Article (Published version)

Identifiers

PID : unige:8082
DOI : 10.1016/S0040-4039(00)92377-3

Journal ISSN0040-4039

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A highly efficient synthesis of (Z) γ-iodo allylic alcohols

The reaction of (Z) Methyl-ß-iodo propenoate with diisobutylaluminium hydride and subsequent reaction with a Grignard reagent allows the synthesis of (Z) ?-iodo allylic alcohols in a very easy way.

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