Issue 4, 1978

Enamine chemistry. Part 24. 2,2-versus 2,6-Disubstitution in 2-alkylcyclohexanone enamines. Factors affecting the regioselectivity and stereoselectivity of enamine alkylation and protonation

Abstract

The factors affecting the reversibility and energetics of competing reaction pathways are discussed and shown to provide a rational explanation for the regioselectivity of reaction of 2-substituted cyclohexanone enamines.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1978, 340-347

Enamine chemistry. Part 24. 2,2-versus 2,6-Disubstitution in 2-alkylcyclohexanone enamines. Factors affecting the regioselectivity and stereoselectivity of enamine alkylation and protonation

P. W. Hickmott and N. F. Firrell, J. Chem. Soc., Perkin Trans. 1, 1978, 340 DOI: 10.1039/P19780000340

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