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