Issue 16, 1970

Stereospecific halogenolysis of β-styrylpyridinecobaloximes. A new general synthesis of isomeric β-halogenostyrenes

Abstract

Both cis- and trans-β-styrylpyridinecobal-oximes react by electrophilic substitution with elemental halogens in acetic acid to give the corresponding cis- and trans-β-halogeno-styrenes in high yields and with complete retention of configuration.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1027-1028

Stereospecific halogenolysis of β-styrylpyridinecobaloximes. A new general synthesis of isomeric β-halogenostyrenes

M. D. Johnson and B. S. Meeks, J. Chem. Soc. D, 1970, 1027 DOI: 10.1039/C29700001027

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