ASYMMETRIC CONJUGATE ADDITION OF ZINCATES OR CUPRATES CONTAINING AN OPTICALLY ACTIVE AZAENOLATE OF erythro-ISOPROPYLIDENE-2-METHOXY-1,2-DIPHENYLAMINE TO 2-CYCLOALKENONES

DOI: 10.1016/S0040-4039(01)91370-X

Source and publish data:

Tetrahedron Letters p. 6347 - 6350 (1987)

Update date:2022-09-26

Topics:

Authors:

Yamamoto, Keiji

Kanoh, Mikiya

Yamamoto, Norio

Tsuji, Jiro

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Article abstract of DOI:10.1016/S0040-4039(01)91370-X

Asymmetric conjugate addition to prochiral cycloalkenones was examined by utilizing a zinc azaenolate as well as a copper one derived from an acetone imine of optically active erythro-2-methoxy-1,2-diphenylethylamine, the best enantioselectivity of the re

Full text of DOI:10.1016/S0040-4039(01)91370-X

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