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  <identifier identifierType="DOI">10.18453/rosdok_id00000623</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Karapetyan, Vahuni</creatorName>
      <givenName>Vahuni</givenName>
      <familyName>Karapetyan</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/140505830</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Synthesis of Bridged and Non-Bridged N-Heterocycles, Dichloromethyl- and Formyl-Salicylates, Pyran-4-ones,Chromanes and Isochromanes based on Cyclocondensation Reactions of 1,3-Bis(silyloxy)-1,3-butadienes and Oxime Dianions</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2009</publicationYear>
  <resourceType resourceTypeGeneral="Text" />
  <subjects>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">540 Chemistry &amp; allied sciences</subject>
  </subjects>
  <dates>
    <date dateType="Created">2009</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00000623</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2010-0033-9</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">Regioselective cyclization reactions of 1,3-bis(silyloxy)-1,3-butadienes provide an elegant approach for the synthesis of various complex carba- and heterocycles. Thus, various bridged and non-bridged N-heterocycles, functionalized salicylates and pyran-4-ones are prepared based on cyclization reactions of 1,3-bis(silylenol ethers). Isochromanes and chromanes are prepared based on chelation-controlled cyclization of 1,3-bis(silylenol ethers) with 1,1-diacylcyclopropanes. In addition, 6-halomethyl-5,6-dihydro-4H-1,2-oxazines are synthesized by regioselective cyclization of arylalkenyl-oximes.</description>
  </descriptions>
</resource>
