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Water promoted allylic nucleophilic substitution reactions of (E)-1,3 diphenylallyl acetate
Journal article   Peer reviewed

Water promoted allylic nucleophilic substitution reactions of (E)-1,3 diphenylallyl acetate

Seema A. Ghorpade, Dinesh N. Sawant, Arwa Makki, Nagaiyan Sekar and Jorg Eppinger
Green chemistry : an international journal and green chemistry resource : GC, Vol.20(2), pp.425-430
2018

Abstract

Chemistry Chemistry, Multidisciplinary Green & Sustainable Science & Technology Physical Sciences Science & Technology Science & Technology - Other Topics
A transition metal free, water based, greener protocol for the allylic alkylation, allylic amination, O-allylation of (E)-1,3-diphenylallyl acetate is described. The developed methodology is applicable for a wide range of nucleophiles furnishing excellent yields of corresponding products up to 87% under mild reaction conditions. A distinct effect of water and base is explored for allylic nucleophilic substitution reactions of (E)-1,3-diphenylallyl acetate.

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