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  <titleInfo>
    <title>Molecular rearrangements in organic synthesis</title>
  </titleInfo>
  <name type="personal">
    <namePart>Rojas, Christian Miguel</namePart>
    <role>
      <roleTerm type="text">editor.</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <genre authority="">Electronic books.</genre>
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      <placeTerm type="code" authority="marccountry">nju</placeTerm>
    </place>
    <dateIssued encoding="marc">2015</dateIssued>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
    <form authority="gmd">electronic resource</form>
    <extent>1 online resource.</extent>
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  <abstract>Designed for practitioners of organic synthesis, this book helps chemists understand and take advantage of rearrangement reactions to enhance the synthesis of useful chemical compounds. -Provides ready access to the genesis, mechanisms, and synthetic utility of rearrangement reactions -Emphasizes strategic synthetic planning and implementation -Covers 20 different rearrangement reactions -Includes applications for synthesizing compounds useful as natural products, medicinal compounds, functional materials, and physical organic chemistry.</abstract>
  <tableOfContents>1,2-migrations. Pinacol and semi-pinacol rearrangements in total synthesis -- Baeyer-Villiger (BV) oxidation/rearrangement in organic synthesis -- The Wolff rearrangement : tactics, strategies and recent applications in organic synthesis -- Alkyl and acyl azide rearrangements -- Beckmann rearrangements and fragmentations in organic synthesis -- Brook rearrangement. 1,2-migrations via three-membered rings. The quasi-favorskii rearrangement -- The Ramberg-Backlund reaction -- Applications of di-pi-methane and related rearrangement reactions in chemical synthesis. 1,3-transpositions. Payne rearrangement -- Vinylcyclopropane-cyclopentene rearrangement -- Ferrier carbocyclization reaction. [3,3]- and [2,3]-sigmatropic rearrangements. The Claisen rearrangement -- [3,3]-sigmatropic rearrangements with heteroatom-heteroatom bonds -- [2,3]-rearrangements of ammonium zwitterions -- Oxonium ylide rearrangements in synthesis -- The [2,3]-Wittig rearrangement -- The Mislow-Evans rearrangement. Ipso rearrangements. Smiles rearrangements -- Pummerer-type reactions as powerful tools in organic synthesis.</tableOfContents>
  <note type="statement of responsibility">edited by Christian M. Rojas.</note>
  <note>Includes bibliographical references and index.</note>
  <subject authority="lcsh">
    <topic>Rearrangements (Chemistry)</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Organic compounds</topic>
    <topic>Synthesis</topic>
  </subject>
  <subject authority="bisacsh">
    <topic>SCIENCE</topic>
    <topic>Chemistry</topic>
    <topic>Organic</topic>
  </subject>
  <subject authority="fast">
    <topic>Organic compounds</topic>
    <topic>Synthesis</topic>
  </subject>
  <subject authority="fast">
    <topic>Rearrangements (Chemistry)</topic>
  </subject>
  <classification authority="lcc">QD281.R35</classification>
  <classification authority="ddc" edition="23">547/.2</classification>
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    <titleInfo>
      <title>Molecular rearrangements in organic synthesis</title>
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    <originInfo>
      <publisher>Hoboken, New Jersey : John Wiley &amp; Sons, Inc., 2015</publisher>
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    <identifier type="local">(DLC)  2015013578</identifier>
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  <identifier type="isbn">9781118939895</identifier>
  <identifier type="isbn">1118939891</identifier>
  <identifier type="isbn">9781118939888</identifier>
  <identifier type="isbn">1118939883</identifier>
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  <identifier type="isbn">9781118347966</identifier>
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  <identifier type="lccn">2015017259</identifier>
  <identifier type="uri">http://onlinelibrary.wiley.com/book/10.1002/9781118939901</identifier>
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    <recordCreationDate encoding="marc">150430</recordCreationDate>
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    <recordIdentifier source="OCoLC">ocn908287097</recordIdentifier>
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