<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 5 Issue 3</issue_number>
<issue_period>2014 (July- September)</issue_period>
<title>SYNTHESIS, CHARACTERIZATION, AND BIOLOGICAL EVALUATION OF AZETIDINONES BY MODIFYING THE PHARMACOPHORIC SITES USING BETTI'S PROTOCOL OF 8-HYDROXYQUINOLINE PRECURSOR </title>
<abstract>An efficient synthesis of series of different novel  lessThan i greaterThan β lessThan /i greaterThan -lactams via cycloaddition reaction (Staudinger reaction) of Schiff base has been reported in the present communication. A series of newly substituted 8-hydroxyquinoline Schiff base derivatives have been synthesized efficiently following Betti's condensation protocol with 8-hydroxyquinoline and different aldehydes under ambient reaction conditions. The structures of the newly synthesized Schiff base derivatives and  lessThan i greaterThan β lessThan /i greaterThan -lactams were confirmed by IR,  lessThan sup greaterThan 1 lessThan /sup greaterThan H NMR, elemental analysis and mass spectroscopic data. In-vitro anti-bacterial evaluations of β-lactams were done against gram-positive and gram-negative bacterial strains using the well diffusion method. It has been observed that some of these derivatives posses potent anti-bacterial characteristics against these bacteria.</abstract>
<authors>HIMANI N. CHOPDE</authors>
<keywords>Azetidinone, 8-hydroxyquinoline, bettiâ€™s condensation, staudinger reaction, schiffâ€™s base, anti-bacterial activity.</keywords>
<pages>541-548</pages>
</article>
</Journal>
