Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/15195
Title: <span style="font-size:12.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-ansi-language: EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB">Synthesis, characterisation and antimicrobial activity of 3-methyl-6-(aryl)-1-phenyl-1<i style="mso-bidi-font-style:normal">H</i>-pyrazolo[3,4-<i style="mso-bidi-font-style: normal">b</i>]pyridine</span>
Authors: Girisha, K S
Kalluraya, Balakrishna
Vidyashree, Jois H S
Keywords: 5-Azidopyrazole
Pyrazolopyridines
<i style="mso-bidi-font-style:normal"><span style="font-size:10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-gb;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa"="" lang="EN-GB">In situ</span></i><span style="font-size: 10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"> Friedlaender reaction</span>
Antimicrobial activity
Issue Date: Dec-2012
Publisher: NISCAIR-CSIR, India
Abstract: A series of 3-methyl-6-(aryl)-1-phenyl-1<i style="mso-bidi-font-style:normal">H</i>-pyrazolo[3,4-<i style="mso-bidi-font-style:normal">b</i>]pyridine have been synthesized in one step by treating 5-azido-3-methyl-1-phenyl-1<i style="mso-bidi-font-style:normal">H</i>-pyrazol-4-carboxaldehyde with suitably substituted acetophenones in basic medium. This reaction is a good example for <i style="mso-bidi-font-style:normal">in situ</i> Friedlaender reaction. The newly synthesized compounds have been screened for their anti-microbial studies. All the compounds show MIC at low concentration itself against the tested fungi.
Description: 1767-1770
URI: http://hdl.handle.net/123456789/15195
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.51B(12) December 2012]

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