Abstract:
The UV irradiation of 2- and 3-methylindoles in acetic acid leads to the formation of the corresponding indole-carboxaldehydes as the major products, whereas the employment of ethanol as solvent causes the cleavage of the C22-C3 bond, giving o-acylaminophenylketones. Some aspects of these photo-reactions are discussed. © 1973.
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Citas:
---------- APA ----------
Mudry, C.A. & Frasca, A.R.
(1973)
. Photo-oxidation of indole derivatives. Tetrahedron, 29(4), 603-613.
http://dx.doi.org/10.1016/0040-4020(73)85002-1---------- CHICAGO ----------
Mudry, C.A., Frasca, A.R.
"Photo-oxidation of indole derivatives"
. Tetrahedron 29, no. 4
(1973) : 603-613.
http://dx.doi.org/10.1016/0040-4020(73)85002-1---------- MLA ----------
Mudry, C.A., Frasca, A.R.
"Photo-oxidation of indole derivatives"
. Tetrahedron, vol. 29, no. 4, 1973, pp. 603-613.
http://dx.doi.org/10.1016/0040-4020(73)85002-1---------- VANCOUVER ----------
Mudry, C.A., Frasca, A.R. Photo-oxidation of indole derivatives. Tetrahedron. 1973;29(4):603-613.
http://dx.doi.org/10.1016/0040-4020(73)85002-1