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  <titleInfo>
    <title>Isocyanide Chemistry</title>
    <subTitle>Applications in Synthesis and Materials Science</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Nenajdenko, Valentine.</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <genre authority="">Electronic books.</genre>
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    <place>
      <placeTerm type="text">Weinheim</placeTerm>
    </place>
    <publisher>Wiley-VCH</publisher>
    <dateIssued>2012</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <extent>1 online resource (xviii, 605 pages) : illustrations</extent>
  </physicalDescription>
  <abstract>The efficacy of isocyanide reactions in the synthesis of natural or naturallike products has resulted in a renaissance of isocyanide chemistry. Now isocyanides are widely used in different branches of organic, inorganic, coordination, combinatorial and medicinal chemistry. This invaluable reference is the only book to cover the topic in such depth, presenting all aspects of synthetic isonitrile chemistry. The highlyexperienced and internationally renowned editor has brought together an equally distinguished team of authors who cover multicomponentreactions, isonitriles in total.</abstract>
  <tableOfContents>1.5.1 Isolation and Natural Sources1.5.2 Synthesis of Naturally Occurring Isocyanides; 1.6 Isocyanides Used in the Synthesis of Chiral Polyisocyanides; 1.6.1 Properties; 1.6.2 Synthesis; 1.6.3 Applications; References; 2: General Aspects of Isocyanide Reactivity; 2.1 Introduction; 2.2 Isocyanide-Cyanide Rearrangement; 2.3 Oxidation/Reduction of the Isocyano Group; 2.3.1 Oxidation of the Isocyano Group; 2.3.2 Reactions with Sulfur and Selenium; 2.3.3 Reduction of the Isocyano Group; 2.4 Reactions of Isocyanides with Electrophiles; 2.4.1 Reaction with Acids.</tableOfContents>
  <note type="statement of responsibility">edited by Valentine Nenajdenko.</note>
  <note>Includes bibliographical references and index.</note>
  <subject authority="lcsh">
    <topic>Isocyanides</topic>
    <topic>Synthesis</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Chemistry, Organic</topic>
  </subject>
  <subject>
    <topic>Bioorganic chemistry</topic>
  </subject>
  <subject>
    <topic>Complex compounds</topic>
  </subject>
  <subject>
    <topic>Isocyanides</topic>
  </subject>
  <subject>
    <topic>Organometallic compounds</topic>
  </subject>
  <subject authority="bisacsh">
    <topic>SCIENCE</topic>
    <topic>Chemistry</topic>
    <topic>Organic</topic>
  </subject>
  <subject authority="gnd">
    <topic>Isocyanide</topic>
  </subject>
  <classification authority="lcc">QD412.C15 I86 2012eb</classification>
  <classification authority="ddc" edition="23">547/.044</classification>
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    <titleInfo>
      <title>Isocyanide chemistry</title>
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    <originInfo>
      <publisher>Weinheim : Wiley-VCH, 2012</publisher>
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    <identifier type="local">(OCoLC)794035539</identifier>
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  <identifier type="stock number">385473 MIL</identifier>
  <identifier type="uri">http://onlinelibrary.wiley.com/book/10.1002/9783527652532</identifier>
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    <recordIdentifier source="OCoLC">ocn802291228</recordIdentifier>
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