Issue 14, 1969

Formation of 1,2- and 1,4-cyclo-adducts from tetrafluorobenzyne and NN-dimethylaniline and a Stevens rearrangement with aryl migration

Abstract

Tetrafluorobenzyne reacts with NN-dimethylaniline to give 1,2- and 1,4-cyclo-adducts and solvent dependent products derived from an intermediate betaine.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 810-810

Formation of 1,2- and 1,4-cyclo-adducts from tetrafluorobenzyne and NN-dimethylaniline and a Stevens rearrangement with aryl migration

H. Heaney and T. J. Ward, J. Chem. Soc. D, 1969, 810 DOI: 10.1039/C29690000810

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