Issue 12, 1970

Cyclic transition states in cis- and trans-addition of chlorine acetate to olefinic substances

Abstract

The stereochemical courses of additions of chlorine acetate to some aryl-substituted unsaturated compounds are markedly less stereoselective than the corresponding reactions initiated by electrophilic chlorine.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 731-732

Cyclic transition states in cis- and trans-addition of chlorine acetate to olefinic substances

P. B. D. de la Mare, C. J. O'Connor, M. J. Rosser and M. A. Wilson, J. Chem. Soc. D, 1970, 731 DOI: 10.1039/C29700000731

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