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N-allylation and N-benzylation of 2-phenylindole and its condensation with carbonyl compounds
Authors:A. A. Obynochnyi  B. N. Anisimov  N. D. Sergeeva  N. S. Prostakov
Affiliation:(1) Russian University of People's Friendship, 117923 Moscow
Abstract:By allylation and benzylation of 2-phenyl- and 2-phenyl-3-formylindole, N-allyl- and benzyl-substituted indoles have been obtained. By condensation of 2-phenylindole with 2-formylfluorene, and also with 4-aza- or 3-methyl-2-azafluorenone, compounds containing fragments of the indole, fluorene, and azafluorenone systems have been synthesized. In the interaction of 2-phenylindole or indole with formaldehyde and 2,5-dimethylpiperidin-4-one, depending on the temperature, bis(2-phenylindol-3-yl)methane, (2prime,5prime-dimethyl-4prime-oxopiperidino)-(1-indolyl)methane, and bis(indol-3-yl)methane are formed.Translated from Khimiya Geterotsiklicheskikh Soedinenii, Vol. 29, No. 5, pp. 648–650, May, 1993.
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