Oxidative Addition of N-Aminophthalimide to Conjugated and Nonconjugated Alkylazoalkanes
MA Kuznetsov, VN Belov, SM Buchaka
Index: Kuznetsov; Belov; Buchaka Russian Journal of Organic Chemistry, 2005 , vol. 41, # 2 p. 204 - 213
Full Text: HTML
Citation Number: 3
Abstract
Abstract A series of γ, δ-unsaturated azo compounds was prepared by thermal isomerization of allylalkylhydrazones obtained from the simplest carbonyl compounds. The oxidation of N- aminophthalimide with lead tetraacetate in the presence of these unsaturated compounds gave rise to mixtures of adducts at the azo group, regioisomers of phthalimidoazimines. The oxidative addition of N-aminophthalimide to 1-isopropylazocycloalkenes afforded bicyclic ...
Related Articles:
[Renger,B.; Seebach,D. Chemische Berichte, 1977 , vol. 110, p. 2334 - 2354]