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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2016-02-02</publicationDate>
    
        <volume>4</volume>
        <issue>1</issue>

 
    <startPage>325</startPage>
    <endPage>328</endPage>

	    <publisherRecordId>5801</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis and biological screening of 2,5 -disubstituted 1,3,4 oxadiazole derivatives</title>

    <authors>
	 


      <author>
       <name>Gautam</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>A.K. Jain</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Kuldeep Singh</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Jagbir </name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>V.K. Singh</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Institute of Pharmacy Bundelkhand University, Jhansi - 284 128 (India)</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Synthesis of a number of 1,3,4 – oxadiazole derivatives have been described. Benztriazole reacting with ethylcholoro acetate in the presence of potassium carbonate to produce ethyl 2 – (1H benzo[d][1,2,3] triazol – 1 yl] acetate ) which further react with hydrazine hydrate to produced (2H-benzo [d][123] triazole – 1 yl aceto hydrazide ] and this react with different aromatic acid in presence of phosphorus oxychloriede offerda 2,5 disubstituted 1,3,4 oxadiazole derivatives. Compounds were tested for antibacterial and antifungal activity.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol4no1/synthesis-and-biological-screening-of-25-disubstituted-134-oxadiazole-derivatives/</fullTextUrl>



      <keywords language="eng">
        <keyword>1</keyword>
      </keywords>

      <keywords language="eng">
        <keyword>3</keyword>
      </keywords>

      <keywords language="eng">
        <keyword>4 – oxadiazole derivatives and antimicrobial activity.</keyword>
      </keywords>

  </record>
</records>