Abstract
Reaction of
methyl-substituted 5-amino-1,4-naphthoquinones with piperidine gave
preferentially 3-piperidino derivatives. The corresponding orientation also
resulted from amination of the dihydroperimidinone
system (1), a slower process. When position 3 of the naphthoquinone was
substituted by a methyl group, preferential side-chain amination of that group
was observed.
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献