Abstract
Potassium carbonate is a remarkable base in the Wittig reaction. It promotes the formation of ethylenic compounds in excellent yields, by a biphasic solid-liquid process. There is modest reactivity in the presence of hydroxides. The Z-isomer is the major product in aprotic media whereas the E-isomer is promoted in protic media. The addition of phase-transfer agents accelerates the reaction. However sodium hydroxide on alumina can be used as the basic system for the Wittig reaction. ©ARKAT.
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Moussaoui, Y., Saïd, K., & Salem, R. B. (2006). Anionic activation of the Wittig reaction using a solid-liquid phase transfer: Examination of the medium-, temperature-, base- and phase-transfer catalyst effects. Arkivoc, 2006(12), 1–22. https://doi.org/10.3998/ark.5550190.0007.c01
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