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Scientific article
English

Enantioselective catalytic rearrangement of cyclohexene oxide with new homochiral bis-lithium amide bases

Published inTetrahedron: asymmetry, vol. 15, no. 7, p. 1069-1072
Publication date2004
Abstract

Cyclohexene oxide can be rearranged with good levels of induction (up to 68% ee) with substoichiometric amounts of chiral bases derived from readily available diamines. The influence of the steric bulk of the amine substituents on the rearrangement enantioselectivity has also been studied.

Citation (ISO format)
EQUEY, Olivier, ALEXAKIS, Alexandre. Enantioselective catalytic rearrangement of cyclohexene oxide with new homochiral bis-lithium amide bases. In: Tetrahedron: asymmetry, 2004, vol. 15, n° 7, p. 1069–1072. doi: 10.1016/j.tetasy.2004.02.030
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ISSN of the journal0957-4166
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