Issue 15, 1974

Electronegatively substituted bicyclobutanes via the cycloaddition of trisubstituted electron-poor olefins to enamines

Abstract

Cycloaddition of trisubstituted electron-poor olefins such as trimethylethylenetricarboxylate to enamines such as N,N-dimethylisobutenylamine, quaternization, and base-induced elimination lead to electronegatively substituted bicyclobutanes such as trimethyl 4,4-dimethylbicyclobutane-1,2,2-tricarboxylate.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 587-588

Electronegatively substituted bicyclobutanes via the cycloaddition of trisubstituted electron-poor olefins to enamines

H. K. Hall and P. Ykman, J. Chem. Soc., Chem. Commun., 1974, 587 DOI: 10.1039/C39740000587

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