Carbenoid Formation of Arylcyclopropanes from Olefins, Benzal Bromides, and Organolithium Compounds and from Photolysis of Aryldiazomethanes
GL Closs, RA Moss
Index: Closs,G.L.; Moss,R.A. Journal of the American Chemical Society, 1964 , vol. 86, p. 4042 - 4053
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Citation Number: 267
Abstract
A number of arylcyclopropanes have been prepared by the reaction of benzal bromide with alkyllithium in the presence of olefins. The same cyclopropanes have also been isolated from the photolysis of the corresponding aryldiazomethanes in olefins. Aryl substituents investigated include p-methyl, p-methoxy, p-chloro, and m-chloro. Olefins used as substrates were 1-butene, isobutene, cis-and trens-2-butene, and 2-methyl-2-butene. Relative rates ...
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