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  <titleInfo>
    <title>Progress in heterocyclic chemistry : Vol. 27</title>
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    <namePart>Gribble, Gordon W.</namePart>
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  <name type="personal">
    <namePart>Joule, J. A. (John Arthur)</namePart>
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    <publisher>Elsevier</publisher>
    <dateIssued>�2015</dateIssued>
    <dateIssued encoding="marc">2015</dateIssued>
    <issuance>monographic</issuance>
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    <extent>1 online resource (xv, 627 pages).</extent>
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  <tableOfContents>Front Cover; PROGRESS IN HETEROCYCLIC CHEMISTRY; Copyright; CONTENTS; CONTRIBUTORS; FOREWORD; EDITORIAL ADVISORY BOARD MEMBERS PROGRESS IN HETEROCYCLIC CHEMISTRY; 1 -- Propargyl Vinyl Ethers as Powerful Starting Points for Heterocycle Synthesis; 1.1 INTRODUCTION; 1.2 SYNTHESIS OF FURANS AND PYRROLES VIA PROPARGYL CLAISEN REARRANGEMENT; 1.3 SYNTHESIS OF 1,3-OXAZOLIDINES VIA MICROWAVE SYNTHESIS; 1.4 SYNTHESIS OF 2H-PYRANS AND 1,2-DIHYDROPYRIDINES; 1.5 SUMMARY; REFERENCES; 2 -- Recent Progress of Phosphonium Coupling in Heterocyclic and Medicinal Chemistry; 2.1 INTRODUCTION.</tableOfContents>
  <tableOfContents>2.2 DISCOVERY OF PHOSPHONIUM COUPLING2.2.1 Phosphonium Salts; 2.2.2 Tautomerizable Heterocycles; 2.2.3 Reaction Discovery; 2.2.4 Solvent Effect and Base Effect; 2.2.5 Reaction Mechanism; 2.3 PHOSPHONIUM COUPLING FOR DIRECT AMINATION; 2.3.1 Direct Amination; 2.3.2 Recent Progress and Application; 2.4 PHOSPHONIUM COUPLING FOR DIRECT ETHERIFICATION; 2.4.1 Direct Etherification; 2.4.2 Recent Progress and Application; 2.5 PHOSPHONIUM COUPLING FOR DIRECT THIOETHERIFICATION; 2.5.1 Direct Thioetherification; 2.5.2 Recent Progress and Application.</tableOfContents>
  <tableOfContents>2.6 PHOSPHONIUM COUPLING FOR DIRECT ALKYLATION2.6.1 Direct Alkylation; 2.6.2 Recent Progress and Application; 2.7 PHOSPHONIUM COUPLING FOR DIRECT ARYLATION; 2.7.1 Direct Arylation; 2.7.2 Reaction Mechanism; 2.7.3 Recent Progress and Application; 2.8 PHOSPHONIUM COUPLING FOR DIRECT ALKYNYLATION; 2.8.1 Direct Alkynylation; 2.8.2 Reaction Mechanism; 2.8.3 Recent Progress and Application; 2.9 PHOSPHONIUM COUPLING FOR NUCLEOSIDE CHEMISTRY; 2.9.1 Multistep Transformation; 2.9.2 Single Step Transformation; 2.10 SUMMARY; REFERENCES; 3 -- Three-Membered Ring Systems; 3.1 INTRODUCTION.</tableOfContents>
  <tableOfContents>5.1.1 INTRODUCTION5.1.2 SYNTHESIS OF THIOPHENES, SELENOPHENES, AND TELLUROPHENES; 5.1.3 ELABORATION OF THIOPHENES AND BENZOTHIOPHENES; 5.1.4 SYNTHESIS OF THIOPHENES, SELENOPHENES, AND TELLUROPHENES FOR THE USE IN THE MATERIAL SCIENCES; 5.1.5 THIOPHENE, SELENOPHENE, AND TELLUROPHENE DERIVATIVES IN MEDICINAL AND ENVIRONMENTAL CHEMISTRY; REFERENCES; 5.2 -- Five-Membered Ring Systems: Pyrroles and Benzo Analogs; 5.2.1 INTRODUCTION; 5.2.2 SYNTHESIS OF PYRROLES; 5.2.2.1 Intramolecular Approaches to Pyrroles; 5.2.2.1.1 Intramolecular Type a; 5.2.2.1.2 Intramolecular Type c.</tableOfContents>
  <note type="statement of responsibility">edited by Gordon W. Gribble, John A. Joule.</note>
  <note>Includes index.</note>
  <note>Includes bibliographical references at the end of each chapters and index.</note>
  <subject authority="lcsh">
    <topic>Heterocyclic chemistry</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Heterocyclic compounds</topic>
    <topic>Congresses</topic>
  </subject>
  <subject authority="bisacsh">
    <topic>SCIENCE</topic>
    <topic>Chemistry</topic>
    <topic>Organic</topic>
  </subject>
  <subject authority="fast">
    <topic>Heterocyclic chemistry</topic>
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  <subject authority="fast">
    <topic>Heterocyclic compounds</topic>
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  <classification authority="lcc">QD399</classification>
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      <publisher>: Elsevier Science, �2015</publisher>
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      <title>Progress in Heterocyclic Chemistry</title>
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