Thermolysis and photolysis of arylchlorodiazirines ...



Title Thermolysis and photolysis of arylchlorodiazirines in allyl bromide
Author(s) R. Bonneau, M. Grobys, Michael T. H. Liu, M. Himori, K. Fukushima, T. Ibata
Journal Research on Chemical Intermediates
Date 1994
Volume 20
Issue 2
Start page 141
End page 148
Abstract p-Chlorophenylchlorocarbene reacts with allyl bromide to form the expected cyclopropanes. In the case of p-nitrophenylchlorocarbene, a small amount of insertion product is also formed in addition to the cycloadducts. The formation of the insertion product is attributed to the attack of the carbene on the bromine atom followed by intramolecular allylic rearrangement.

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