Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16611
Title: Microwave-induced synthesis of nitrogen-mustard derivatives
Authors: Kidwai, Mazaahir
Kumar, Rajesh
Kohli, Seema
Issue Date: Sep-1999
Publisher: NISCAIR-CSIR, India
Abstract: N,N-Bis (2-hydroxyethyl) amino substituted propiophenones 2a-c have been prepared using Mannich reaction from substituted acetophenones 1a-c. 2a-c on hydrazinolysis yield 3a-f which on chlorination give nitrogen mustards 4a-f. 4a-f on reaction with chloracetyl chloride, N-methylmorpholine and chlorobenzene under mircrowave activation (MWI) afford β-lactams 5a-f while cyclisation of 4a-f with polyphosphoric acid under MWI give the indoles 6a-f.
Page(s): 1132-1135
Appears in Collections:IJC-B Vol.38B(09) [September 1999]

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