Issue 18, 1969

Acetolysis of phenyl-substitute endo- and exo-bicyclo[n,1,0]alkyl chlorides; evidence for concerted dis(2), nonconcerted dis(0) and partially ring-opened carbonium-ion mechanisms

Abstract

A study of the effect of phenyl-substitution on the rate of reaction and products produced in the acetolysis of bicyclo[n,1,0]alkyl chlorides provides evidence for three different modes of ring-opening in the transformation of the cyclopropyl to allyl system.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 1050-1052

Acetolysis of phenyl-substitute endo- and exo-bicyclo[n,1,0]alkyl chlorides; evidence for concerted dis(2), nonconcerted dis(0) and partially ring-opened carbonium-ion mechanisms

D. T. Clark and G. Smale, J. Chem. Soc. D, 1969, 1050 DOI: 10.1039/C29690001050

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