Mechanism of the benzophenone-sensitized photolysis of O-benzoyl-N-(1- naphthoyl)-N-phenylhydroxylamine in cationic micellar media

DOI: 10.1246/bcsj.72.2771

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2771 - 2780 (1999)

Update date:2022-08-03

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Authors:

Kaneko, Tsuyoshi

Tokue, Tatsuya

Kubo, Kanji

Sakurai, Tadamitsu

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Article abstract of DOI:10.1246/bcsj.72.2771

The benzophenone-sensitized photolysis of the title hydroxylamine (1) in hexadecyltrimethylammonium chloride (HTAC) micelles was found to give benzoyloxy(2,3)- and phenyl(4,5)-migrated products, along with fragmentation products, 1-naphthanilide (6) and b

Full text of DOI:10.1246/bcsj.72.2771

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Product name:1-Naphthalenecarboxamide, N-[1,1'-biphenyl]-2-yl-

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