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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>2015-01-22</publicationDate>
    
        <volume>1</volume>
        <issue>2</issue>

 
    <startPage>293</startPage>
    <endPage>296</endPage>

	    <publisherRecordId>427</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Diastereo selective Synthesis of Phosphonate Ester through the Reaction Between Activated Acetylenic Ester and Heterocyclic NH Compounds with Biological Activity in the Presence of Triphenylphosphite.</title>

    <authors>
	 


      <author>
       <name>Malek Taher Maghsoodlou</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Noroullah Hazeri</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Sayyed Mostafa Habibi Khorassani</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Forough Jalili Milani</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Mohammad Amin Kazemian </name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Mahdi Shahraki</name>

		
	<affiliationId>1</affiliationId>
      </author>
    
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Chemistry, The University of Sistan and Balouchestan, Zahedan (Iran)</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">The reaction between dimethyl acetylenedicarboxylate and biological active heterocyclic NH compounds such as 3-methylpyrazole and 3,6-diboromocarbazole in the presence of triphenylphosphite at room temperature led to phosphonate ester 4a-b. The configuration of compounds 4a-b (2S*,3R*)-were determined on the basis of coupling constants emerged from the Karplus equation.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol1no2/diastereoselective-synthesis-of-phosphonate-ester-through-the-reaction-between-activated-acetylenic-ester-and-heterocyclic-nh-compounds-with-biological-activity-in-the-presence-of-triphenylphosphite/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Diastereo selectivity</keyword>
      

      
        <keyword> Heterocyclic NH compounds</keyword>
      

      
        <keyword> biological activity</keyword>
      

      
        <keyword> Activated acetylenic ester</keyword>
      
</keywords>
  </record>
</records>