Autocatalytic Radical Ring Opening of N??Cyclopropyl??N??phenylamines Under Aerobic Conditions− Exclusive Formation of the Unknown Oxygen Adducts, N??(1, 2?? …
…, HB Wickman, MPD Mahindaratne
Index: Wimalasena, Kandatege; Wickman, Heang B.; Mahindaratne, Mathew P. D. European Journal of Organic Chemistry, 2001 , # 20 p. 3811 - 3817
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Citation Number: 13
Abstract
Abstract In contrast to the high stability of N-alkyl-N-cyclopropylamine derivatives, N- cyclopropyl-N-phenylamine (1a) has been found to slowly convert into the hitherto unknown product N-(1, 2-dioxolan-3-yl)-N-phenylamine (1f) at room temperature under aerobic conditions. The rate of this conversion was found to be significantly increased by the presence of a catalytic amount of the single-electron oxidizing agent tris (1, 10- ...
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[European Journal of Organic Chemistry, , # 20 p. 3811 - 3817]