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|Title:||Synthesis of novel naphtho[2,1-b]furo[3,2-b]pyridine derivatives as potential antimicrobial agents|
Vaidya, V P
|Keywords:||Naphthofuran;Naphthofuropyridine;Thrope-Zielger reaction;Friedlander reaction;Antimicrobial activity|
|Abstract:||The starting materials 2-acyl-3-aminonaphtho[2,1-b]furans 4a-b have been directly synthesized from 2-hydroxy-1-naphthaldehyde oxime by treating with α-haloketone through Thrope-Ziegler reaction. The compounds 4a-b undergo Friedlander cyclization on treatment with active methylene compounds, and produce title compounds 5a-b, 6a-b and 7a-b. Some other routes for the synthesis of various derivatives of this new heterocycle have been investigated. All the newly synthesized compounds are characterized by elemental analysis, spectral studies, and have been evaluated for antimicrobial activity.|
|Appears in Collections:||IJC-B Vol.47B(05) [May 2008]|
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