Issue 4, 1975

Transmission of electronic effects by the oxiran ring. Ionization constants of meta- and para-substituted 2,3-epoxy-3-phenylpropionic acids in 50% ethanol

Abstract

The ionization constants of meta- and para-substituted 2,3-epoxy-3-phenyl propionic acids have been measured in 50% ethanol. The results show that the oxiran ring transmits conjugation slightly better than the cyclopropane ring.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1975, 371-372

Transmission of electronic effects by the oxiran ring. Ionization constants of meta- and para-substituted 2,3-epoxy-3-phenylpropionic acids in 50% ethanol

L. Standoli, J. Chem. Soc., Perkin Trans. 2, 1975, 371 DOI: 10.1039/P29750000371

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