Various alkylcuprates were added to the Z and E vinylogous esters of N,O-diprotected (D) or (L) serinal 1. Good to excellent yields and asymmetric inductions were observed. © 1990.
Jako, I., Uiber, P., Mann, A., Taddei, M., Wermuth, C.G. (1990). Diastereoselectivity In Conjugate Addition of Alkylcuprates To Vinylogous Ester of N,o-diprotected Serinal. TETRAHEDRON LETTERS, 31(7), 1011-1014 [10.1016/S0040-4039(00)94416-2].
Diastereoselectivity In Conjugate Addition of Alkylcuprates To Vinylogous Ester of N,o-diprotected Serinal
Taddei, Maurizio;
1990-01-01
Abstract
Various alkylcuprates were added to the Z and E vinylogous esters of N,O-diprotected (D) or (L) serinal 1. Good to excellent yields and asymmetric inductions were observed. © 1990.
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