Title of article :
Reactivity of benzyl radicals: The trapping of primary, secondary and tertiary benzyl radicals with heterocyclic bases
Author/Authors :
Brivio، نويسنده , , Luigi and Caronna، نويسنده , , Tullio and Fontana، نويسنده , , Francesca and Gambarotti، نويسنده , , Cristian and Mele، نويسنده , , Andrea and Sora، نويسنده , , Isabella Natali and Punta، نويسنده , , Carlo and Recupero، نويسنده , , Francesco، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2010
Pages :
3
From page :
112
To page :
114
Abstract :
A photochemical benzylation of protonated quinolines was realized by single electron transfer (SET) to the excited state of the quinoline from the aromatic reactant. The benzylated product is formed by cross-coupling between the benzyl radical and the heterocyclic radical when they are in close proximity to one another. This allows the formation of products which are, to the best of our knowledge, unaccessible in other ways and which have now been obtained for the first time.
Keywords :
PhotoSET , Benzyl radicals , Benzylquinolines
Journal title :
Journal of Photochemistry and Photobiology:A:Chemistry
Serial Year :
2010
Journal title :
Journal of Photochemistry and Photobiology:A:Chemistry
Record number :
1625758
Link To Document :
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