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Scientific article
English

Catalytic enantioselective deprotonation of meso-epoxides utilising homochiral bis-lithium amide bases

Published inTetrahedron: asymmetry, vol. 8, no. 7, p. 1019-1022
Publication date1997
Abstract

(R)-2-Cyclohexen-1-ol and (R)-2-cyclooctene-1-ol have been prepared in very good ee using R,R-homochiral bis-lithium amide bases derived from homochiral C2 symmetric diamines. (R)-2-Cyclohexen-1-ol has been synthesized in good ee utilising catalytic homochiral bis-lithium amide in the presence of n-butyl lithium.

Affiliation Not a UNIGE publication
Citation (ISO format)
TIERNEY, Jason P., ALEXAKIS, Alexandre, MANGENEY, Pierre. Catalytic enantioselective deprotonation of meso-epoxides utilising homochiral bis-lithium amide bases. In: Tetrahedron: asymmetry, 1997, vol. 8, n° 7, p. 1019–1022. doi: 10.1016/S0957-4166(97)00084-0
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ISSN of the journal0957-4166
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