Tetrahedron Letters p. 4779 - 4782 (1997)
Update date:2022-08-04
Topics:
Kaneko, Tsuyoshi
Kubo, Kanji
Sakurai, Tadamitsu
Analysis of the effects of added benzyl alcohol and a heavy atom (Br-) on the quantum yields for the benzophenone-sensitized reaction of the title hydroxylamine in hexadecyltrimethylammonium chloride micelles revealed that the benzoyloxy-migrated products are derived from the amidyl-benzoyloxyl radical pair that is present at the I micellar surface, whereas the amidyl-phenyl radical pair that is penetrated more deeply into the micellar interior is responsible for the appearance of the phenyl-rearranged products.
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Doi:10.1021/om970347j
(1997)Doi:10.1007/BF00761092
()Doi:10.1016/S0009-2614(97)00700-8
(1997)Doi:10.1080/00945719708000249
(1997)Doi:10.1016/0960-894X(96)00420-9
(1996)Doi:10.1016/S0040-4039(00)72871-1
(1968)
