1968
DOI: 10.1021/ja01014a602
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Additions and Corrections - A Homolytic Mechanism for the Thermal Isomerization and Decomposition of n-Benzhydryl-α,α-diaryl Nitrones

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1973
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“…Configurationally Isomeric Iminoxy Radicals. Intermediates in the Rearrangements of Nitrones to -Alkyl Oximes1 Sir: Previous investigations2 3 of the thermal rearrangement of A-benzhydryla, -diphenylnitrone (1) to benzophenone O-benzhydryloxime (2) provide evidence for a homolytic cleavage to iminoxy and benzhydryl radicals with subsequent recombination at oxygen. 4 We now report evidence which indicates that geometrically isomeric diaryliminoxy radicals (Z)-4 and (E)-4 undergo syn-anti isomerization five or six orders of magnitude faster than the corresponding oxime anions.…”
Section: Vamentioning
confidence: 99%
“…Configurationally Isomeric Iminoxy Radicals. Intermediates in the Rearrangements of Nitrones to -Alkyl Oximes1 Sir: Previous investigations2 3 of the thermal rearrangement of A-benzhydryla, -diphenylnitrone (1) to benzophenone O-benzhydryloxime (2) provide evidence for a homolytic cleavage to iminoxy and benzhydryl radicals with subsequent recombination at oxygen. 4 We now report evidence which indicates that geometrically isomeric diaryliminoxy radicals (Z)-4 and (E)-4 undergo syn-anti isomerization five or six orders of magnitude faster than the corresponding oxime anions.…”
Section: Vamentioning
confidence: 99%