Issue 1, 1988

Rates of enantiomerization of trans-1,2-disubstituted cyclopropanes correlate with substituent radical stabilization energies

Abstract

Experimental ΔG(enantiomerization) values for trans-1,2-disubstituted cyclopropanes correlate in strict linearity with the sum of substituent radical stabilization energy terms; the two ends of the 1,3-disubstituted trimethylene diradicals implicated in these thermal enantiomerization reactions appear to be thermochemically independent.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 31-32

Rates of enantiomerization of trans-1,2-disubstituted cyclopropanes correlate with substituent radical stabilization energies

J. E. Baldwin, J. Chem. Soc., Chem. Commun., 1988, 31 DOI: 10.1039/C39880000031

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