Journal of the Chemical Society. Chemical communications p. 162 - 163 (1981)
Update date:2022-08-10
Topics:
Yamamoto, Yoshinori
Yatagai, Hidetaka
Maruyama, Kazuhiro
Triphenyltin enolates, prepared from lithium enolates and triphenyltin chloride, undergo a rapid aldol condensation with aldehydes without the need for the presence of Lewis acids to give predominantly the erythro-product regardless of the geometry of the starting enolates.
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