Etude du mécanisme de la transformation photochimique d'alkylarènesulfonamido-2 cyclohexène-2 one en alkylamino-2 aryl-3 cyclohexène-2 one
J Cossy, JP Pete
Index: Cossy, Janine; Pete, Jean-Pierre Tetrahedron, 1981 , vol. 37, p. 2287 - 2296
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Abstract
When excited in their triplet excited state 2-arenesulfanamido-2-cyclohexenones lead to a very efficient desulfonation reaction and to migration of the aryl substituent. A wavelength effect was observed on the desulfonation product from direct irradiations. Furthermore, at 254 nm, a concentration effect and a quantum yield higher than unity indicate that a radical chain component was involved. The mechanism of this reaction is discussed taking into ...
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[Arnould, J.C.; Cossy, J.; Pete, J.P. Tetrahedron, 1980 , vol. 36, p. 1585 - 1592]
[Arnould, J.C.; Cossy, J.; Pete, J.P. Tetrahedron, 1980 , vol. 36, p. 1585 - 1592]