Oxidative phenylamination of 5-substituted 1-hydroxynaphthalenes to N-phenyl-1,4-naphthoquinone monoimines by air and light “on water”

A number of N-phenyl-1,4-naphthoquinone monoimines 6–10 were prepared by on-water oxidative phenylamination of 1,5-dihydroxynaphthalene (1) and 5-acetylamino-1-hydroxynaphthalene (5) with oxygen-substituted phenylamines under aerobic conditions and either solar or green LED radiation, in the presenc...

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Bibliografiska uppgifter
I publikationen:Beilstein J Org Chem
Huvudupphovsmän: Benites, Julio, Meléndez, Juan, Estela, Cynthia, Ríos, David, Espinoza, Luis, Brito, Iván, Valderrama, Jaime A
Materialtyp: Artigo
Språk:Inglês
Publicerad: Beilstein-Institut 2014
Ämnen:
Letter
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4222432/
https://ncbi.nlm.nih.gov/pubmed/25383115
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.10.255
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