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Hydrogen abstraction, ketones biradical rearrangements

This mechanism agrees with the primary step in the photoisomerization of both low and high molecular weight o-alkyl ketones, which involves intramolecular hydrogen abstraction by the n-m triplet to form the biradical, which in turn rearranges into the enol [197, 198, 1060, 2200, 2201]. [Pg.121]


See other pages where Hydrogen abstraction, ketones biradical rearrangements is mentioned: [Pg.181]    [Pg.144]    [Pg.159]    [Pg.199]    [Pg.55]    [Pg.222]    [Pg.2068]    [Pg.1098]    [Pg.1181]    [Pg.1439]    [Pg.176]    [Pg.2067]    [Pg.1204]   
See also in sourсe #XX -- [ Pg.58 ]




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