Evidence for reversible ring-opening of the α-cyclopropylbenzyl radical

Abstract
Kinetic absorption spectroscopy, EPR, and tributyistannane product data indicate that the α-cyclopropylbenzyl radical (1a) undergoes reversible ring-opening to the 4-phenylbut-3-enyl radical (2a) and that equilibrium favours the ring-closed form, (1a).

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