<?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 2 Issue 3</issue_number>
<issue_period>2011 (July - September)</issue_period>
<title>Synthesis Of New Pyridine Derivatives As Potent Antifungal Agents. </title>
<abstract>A series of 2-aminomethylene-[2´-(3´´-chloro-2´´-oxo-4´´-substitutedaryl-1´´-azetidinyl)-1´,3´,4´-thiadiazol-5´-yl)pyridines (5a-5g) and 2-aminomethylene-[2´-(2´´-substitutedaryl-4´´-thiazolidinone-3´´-yl)-1´,3´,4´-thiadiazol-5´-yl]pyridines (6a-6g) has been synthesised from 2-aminomethylene-(2´-substitutedarylidineimino-1´,3´,4´-thiadiazol-5´-yl)pyridines (4a-4g). The structures of all these compounds were established on the basis of elemental (C,H,N) and spectral (IR,  lessThan sup greaterThan 1 lessThan /sup greaterThan H-NMR and mass spectral data) analysis. All the compounds were screened for their antifungal activity. Compound 2-aminomethyene-[2´-(2´´-(3-hydroxyphenyl)-4´´-thiazolidinone-3´´-yl)-1´,3´,4´-thiadiazol-5´-yl]pyridines were found to be the most potent compound of the series and its activity was compared with the reference drugs Fluconazole and Gieseofulvin.</abstract>
<authors>Chatrasal Singh Rajput, Sanjeev Sharma# And Yashovardhan</authors>
<keywords>Pyridine, thiadiazole, thiazolidinone,  azetidinone  and antifungal activity. </keywords>
<pages>200-209</pages>
</article>
</Journal>
