Abstract
Under the simultaneous influence of light and an acid, the nitrosamines derived from four heterocyclic amines readily form 1:1 photo-adducts with cyclohexene giving excellent yields of 2-tert-aminocyclohexanone oximes. While N-nitrosodi-n-butylamine, under similar conditions, gives a fair yield of the 1:1 photo-adduct, N-nitrosodicyclohexylamine and N-nitrosodiisopropylamine do not. The conformations of these oximes are discussed in conjunction with the n.m.r. data.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
41 articles.
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