Issue 11, 1999
From the journal:

Journal of Chemical Research, Synopses

Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine

Tsuyoshi Kaneko,   Kanji Kubo  and  Tadamitsu Sakurai  

Abstract

The title hydroxylamine in sodium dodecyl sulfate micelles containing benzophenone is subjected to photorearrangements giving benzoyloxy- and phenyl-migrated products along with fragmentation products; subsequent photohydrolysis of the 1,5-benzoyloxy-rearranged product proceeds selectively.

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Article information

DOI
https://doi.org/10.1039/A905502I
Article type
Paper

J. Chem. Res. (S), 1999, 644-645

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Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine

T. Kaneko, K. Kubo and T. Sakurai, J. Chem. Res. (S), 1999, 644 DOI: 10.1039/A905502I

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