Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22110
Title: Friedel Crafts reaction on [2,3]oxopolymethelene indoles
Authors: Prasad, K J Rajendra
Balamurali, R
Kavitha, C
Issue Date: Nov-2002
Publisher: NISCAIR-CSIR, India
Abstract: 1-Oxo-1,2,3,4-tetrahydrocarbazoles 1a-e and 1-oxo-1,2 ,3,4,5,10- hexahydrocyclohept[b] indoles 1f-j are treated with a mixture of glacial acetic acid and polyphosphoric acid in an expectation to yield 5,6-dihydro-2-methyl-4-oxopyrano[2,3-a]carbazoles 2a-e and 5,6,7,12-tetrahydro-2-methyl-4-oxopyrano[2',3';7,6]cyclohept[b]indoles 2f-j, respectively. Instead, acetyl derivatives of 1a-j are obtained.Their characterization and the effect of the substituents on the reactivity and orientation of the above reaction have been discussed.
Page(s): 2421-2424
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.41B(11) [November 2002]

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