Dimerization of 3,4-disubstituted cinnamic acids and esters

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Abstract

Cinnamic (3-phenylpropenoic) acids and esters bearing hydroxy and/or alkoxy groups at C-3 and C-4 on the benzene ring, 1 undergo cyclodimerization on treatment with trifluoroacetic acid to yield the corresponding [t-3-aryl-c-2-carboxy[or alkoxycarbonyl]-r-1-indanyl]acetic acids or esters 2.

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Al-Farhan, E., Keehn, P. M., & Stevenson, R. (1992). Dimerization of 3,4-disubstituted cinnamic acids and esters. Synthesis, (10), 959–961. https://doi.org/10.1055/s-1992-26278

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