Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/22550
Title: Studies on aroylation of 2,3-pyridinediamines
Authors: Dubey, P K
Kumar, R Vinod
Issue Date: Oct-2000
Publisher: NISCAIR-CSIR, India
Abstract: The reaction of 2,3-pyridinediamine 1a and its 5-bromo analogue 1b, independently, with acid chloride or anhydride does not yield the diaroyl derivative and instead yields the cyclised product 3 or the monoaroyl derivative 4 depending upon the conditions. Studies on the attempted condensation of 4 with acid chlorides have been described and a rational explanation has been offered for the unusual resistance of the 2-amino group of 4 towards further attack by electrophiles.
Page(s): 746-751
URI: http://hdl.handle.net/123456789/22550
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.39B(10) [October 2000]

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