Issue 5, 1970

Enamine chemistry. Part VII. Synthesis and structure of dienamines of 3-alkyl-5,5-dimethylcyclohex-2-enones. Factors affecting the formation and relative stability of exo- and endo-cyclic diene systems

Abstract

Several 3-alkyl-5,5-dimethylcyclohex-2-enones have been prepared and have been shown to give only linear conjugated dienamines. The 1H n.m.r. spectra of the dienamines are reported and the factors which affect the endo-exo-cyclic ratio are discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 716-719

Enamine chemistry. Part VII. Synthesis and structure of dienamines of 3-alkyl-5,5-dimethylcyclohex-2-enones. Factors affecting the formation and relative stability of exo- and endo-cyclic diene systems

N. F. Firrell and P. W. Hickmott, J. Chem. Soc. C, 1970, 716 DOI: 10.1039/J39700000716

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