Tetrahedron Letters p. 3015 - 3018 (1989)
Update date:2022-09-26
Topics:
Riley, Pamela
Hanzlik, Robert P.
Arylcyclopropyl radicals can be formed under mild conditions (phase-transfer-catalyzed chlorination) and give rise to cyclopropyl products; in contrast one-electron oxidation of arylcyclopropanes by Mn(OAc)3 leads to fragmentation of the cyclopropane ring and the formation of acyclic products.
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