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  <Article>
    <Journal>
      <PublisherName>ijesm</PublisherName>
      <JournalTitle>International Journal of Engineering, Science and</JournalTitle>
      <PISSN>I</PISSN>
      <EISSN>S</EISSN>
      <Volume-Issue>Volume 6, Issue 2 </Volume-Issue>
      <PartNumber/>
      <IssueTopic>Multidisciplinary</IssueTopic>
      <IssueLanguage>English</IssueLanguage>
      <Season>June 2017</Season>
      <SpecialIssue>N</SpecialIssue>
      <SupplementaryIssue>N</SupplementaryIssue>
      <IssueOA>Y</IssueOA>
      <PubDate>
        <Year>2017</Year>
        <Month>06</Month>
        <Day>1</Day>
      </PubDate>
      <ArticleType>Engineering, Science and Mathematics</ArticleType>
      <ArticleTitle>__ampersandsignnbsp; __ampersandsignnbsp;SYNTHESIS OF N-SUBSTITUTED HYDROXAMIC ACIDS</ArticleTitle>
      <SubTitle/>
      <ArticleLanguage>English</ArticleLanguage>
      <ArticleOA>Y</ArticleOA>
      <FirstPage>57</FirstPage>
      <LastPage>64</LastPage>
      <AuthorList>
        <Author>
          <FirstName>D. N. Sharma* S. K.</FirstName>
          <LastName>Rajput**</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>N</CorrespondingAuthor>
          <ORCID/>
        </Author>
      </AuthorList>
      <DOI/>
      <Abstract>A series of N-substituted hydroxamic acids, R.N(OH).C(O).R__ampersandsignrsquo;, have been synthesized by reacting freshly prepared N-substituted hydroxylamines and acid chlorides in mixed diethyl ether and petroleum ether (boiling range 40 to 600 C) media at 0 to 50 C, and neutralizing the liberated hydrochloric acid with aqueous suspensions of sodium bicarbonate. These compounds have been prepared for analytical applications and physico-chemical studies. These are also to be examined for antibacterial, antifungieidal and antiviral activity. The melting points of these compounds are as under. R=-C6H4CH3-4, R__ampersandsignrsquo;= -C6H4F-3, 990 : -C6H4Cl-3, 990; -C6H3Cl2-2,4, 1630; -CH2 Cl, 1230; -(CH2)7 CH3, 820; - (CH2)8 CH3, 860; - (CH2)2C6H5, 1180; - (CH)2C6H5, 1560; -(CH3O)2C6H3-3,5, 1300; -C4H3, 1310 R=-C6H4CH3-3, R__ampersandsignrsquo;= -C (CH3)3, 1050 : R=-C6H4Cl-4, R__ampersandsignrsquo;= -(CH2)14CH3, 1000 : R=- CH2C6H5, R__ampersandsignrsquo;= -C (CH3)3, 1040 : -(CH2)14CH3, 940 :</Abstract>
      <AbstractLanguage>English</AbstractLanguage>
      <Keywords>substituted phenyl, 2 – furyl or alkyl group</Keywords>
      <URLs>
        <Abstract>https://www.ijesm.co.in/ubijournal-v1copy/journals/abstract.php?article_id=2873&amp;title=__ampersandsignnbsp;&#13;
&#13;
__ampersandsignnbsp;SYNTHESIS OF N-SUBSTITUTED HYDROXAMIC ACIDS</Abstract>
      </URLs>
      <References>
        <ReferencesarticleTitle>References</ReferencesarticleTitle>
        <ReferencesfirstPage>16</ReferencesfirstPage>
        <ReferenceslastPage>19</ReferenceslastPage>
        <References/>
      </References>
    </Journal>
  </Article>
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