Issue 15, 1969

Concerted and non-concerted transformations of cyclopropyl to allyl; the solvolysis of endo- and exo-7-chloro-7-p-substituted-phenylbicyclo[4,1,0]heptanes

Abstract

Activation parameters have been obtained for the acetolysis of epimeric 7-chloro-7-p-substitutedphenylbicyclo[4,1,0]heptanes; the evidence suggests concerted dis(2) and non-concerted dis(0) modes of ring opening for the endo- and exo-chloro-epimers, respectively.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 868b-870

Concerted and non-concerted transformations of cyclopropyl to allyl; the solvolysis of endo- and exo-7-chloro-7-p-substituted-phenylbicyclo[4,1,0]heptanes

D. T. Clark and G. Smale, J. Chem. Soc. D, 1969, 868b DOI: 10.1039/C2969000868B

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