In the second communication the synthesis of para‐substituted 2‐methyl‐3‐phenylpropen(1)‐carboxylic acid derivatives is described: Phenylacetone compounds are formed by decarboxylation of a glycidicester; these react according to theWadsworth‐Emmons(Wittig‐Horner)‐reaction with the corresponding phosphonates to the title compounds. NMR. data show the formation of the steric isomers of 3‐Phenyl‐2‐methyl‐propen‐1‐ and 3‐Phenyl‐2‐methylpropen‐2‐carboxylic acid derivatives.
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Franke et al. (1975) studied this question.
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