Free radical chlorination and one-electron oxidation of arylcyclopropanes. Designer probes for cytochrome P-450 hydroxylation mechanisms
作者:Pamela Riley、Robert P. Hanzlik
DOI:10.1016/s0040-4039(00)99390-0
日期:1989.1
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.
可以在温和的条件下(相转移催化的氯化)形成芳基环丙基自由基,并生成环丙基产物。相比之下,Mn(OAc)3对芳基环丙烷的单电子氧化会导致环丙烷环断裂并形成无环产物。