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Carbene reactions with cis azo functions. Formation of ester azines from. DELTA. 3-1, 3, 4-oxadiazolines

D Keus, M Kaminski, J Warkentin

文献索引:Keus, Diane; Kaminski, Maciej; Warkentin, John Journal of Organic Chemistry, 1984 , vol. 49, # 2 p. 343 - 347

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被引用次数: 26

摘要

Thermolysis of a 2-alkoxy-2, 5, 5-trialkyl-A3-1, 3, 4-oxadiazoline (l), either neat or in a solvent such as benzene, leads to a carbonyl ylide intermediate which fragments to carbonyl compounds and carbenes. The latter attack the parent oxadiazoline at the azo function, presumably to form azomethine imine ylides. The latter ylides then fragment to form carbonyl compounds and azines such as R1 (R20) C= NN= C (OR2) R1, R1 (R20) C= NN= C (R3) ...

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