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Scientific article
English

Asymmetric cleavage of chiral α,β-ethylenic acetals by organolithium reagents

Published inTetrahedron: asymmetry, vol. 7, no. 12, p. 3343-3346
Publication date1996
Abstract

a,ß-Ethylenic chiral acetals react regio- and stereoselectively with organolithium reagents. The obtained enol ether may be hydrolyzed into a chiral ß-disubstituted aldehyde.

Affiliation Not a UNIGE publication
Citation (ISO format)
ALEXAKIS, Alexandre et al. Asymmetric cleavage of chiral α,β-ethylenic acetals by organolithium reagents. In: Tetrahedron: asymmetry, 1996, vol. 7, n° 12, p. 3343–3346. doi: 10.1016/S0957-4166(96)00438-7
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ISSN of the journal0957-4166
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