Issue 3, 1979

Difference between the acidities of cis- and trans-hydrogens at a cyclopropane ring carbon

Abstract

Results from deuterium exchange experiments indicate that the acidity of 1-H of cis-1-acetyl-2-phenylcyclopropane is much higher than that of 1-H of the trans-isomer; this agrees with results of CNDO/2 calculations.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 101-102

Difference between the acidities of cis- and trans-hydrogens at a cyclopropane ring carbon

O. Itoh, N. Yamamoto, H. Fujimoto and K. Ichikawa, J. Chem. Soc., Chem. Commun., 1979, 101 DOI: 10.1039/C39790000101

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