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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2015-01-20</publicationDate>
    
        <volume>1</volume>
        <issue>1</issue>

 
    <startPage>51</startPage>
    <endPage>60</endPage>

	    <publisherRecordId>204</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of Heterocyclic Stable Phosphorus Ylides from Reaction Between Triphenylphosphine and Activated Acetylenic Esters in the Presence of Biological Active NH Heterocyclic Compounds</title>

    <authors>
	 


      <author>
       <name>Malek Taher Maghsoodlou</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Reza Heydari</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Norollah Hazer</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name> Sayyed Mostafa Habibi-Khorassani</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Mahmoud Nassiri</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Mohammad Amin Kazemian</name>

		
	<affiliationId>1</affiliationId>
      </author>
    
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Chemistry, The University of Sistan and Balouchestan.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Triphenylphosphine reacts with dialkyl acetylenedicarboxylates in the presence of biological active NH heterocyclic compounds, such as (2H) -3-pyridazinone, 1-phenyl-3-pyrazolid- inone, 2,4-thiazolinedione, Rhodanine, 4,5,6,7-tetrahydroindazole and 3-methyl- pyrazole to generate stable phosphorus ylides. These compounds exist in solution as a mixture of two geometrical isomers as a result of restricted rotation around the carbon-carbon partical double bond resulting from conjugation of the ylide moiety with the adjacent carbonyl group.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol1no1/synthesis-of-heterocyclic-stable-phosphorus-ylides-from-reaction-between-triphenylphosphine-and-activated-acetylenic-esters-in-the-presence-of-biological-active-nh-heterocyclic-compounds/</fullTextUrl>

<keywords language="eng">

      
        <keyword><b> </b>Activated acetylenic esters</keyword>
      

      
        <keyword> NH heterocyclic compounds</keyword>
      

      
        <keyword> Triphenyl- phosphine</keyword>
      
</keywords>
  </record>
</records>