Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21720
Title: Electrophilic substitution of indoles : Part XXI - Further investigation on the formation of the benzazepinone skeleton
Authors: Banerji, J
Chatterjee, A
Saha, M
Mukherjee, P
Kanrar, S
Issue Date: Oct-2003
Publisher: NISCAIR-CSIR, India
Abstract: An interesting observation was made during the electrophilic substitution of indole with 5,5-dimethyl cyclohexane 1,3-dione resulting in the synthesis of 2,3,4,5, 10,11- hexahydro-3,3-dimelhyl-11- (indo-3-yl)-dibenz-[b,f]azepine-1-one system. The reactions with 2-methyl- and 3-methyl indoles resulted in the formation of only the 1:1 product. The structures of the products have been settled on the basis of their UV, IR.1H and 13C NMR spectral studies and MS analysis.
Page(s): 2573-2576
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.42B(10) [October 2003]

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