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  <identifier identifierType="DOI">10.18453/rosdok_id00001536</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Abbasi, Muhammad Shakeel Ahmed</creatorName>
      <givenName>Muhammad Shakeel Ahmed</givenName>
      <familyName>Abbasi</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1071809431</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Annulation reactions of heterocyclic chlorovinyl-aldehydes</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2015</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">2015</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00001536</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-diss2015-0086-0</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">A simple and convenient domino cycloaromatization approach towards the synthesis of novel benzo[c]chromen-6-ones and benzo[c]chromenes by treatment of heterocyclic chlorovinyl-aldehydes with active methylene compounds has been developed. In another strategy novel biaryl lactones were prepared by Sonogashira cross-coupling and base catalyzed reactions of 4-chloro-2-oxo-2H-chromene-3-carbaldehyde with terminal alkynes and 1, 3-dicarbonyl compounds.Finally some heterocyclic chlorovinyl-aldehydes were treated with electron rich heterocyclic amines to afford novel heteroannulated  pyridines.</description>
  </descriptions>
</resource>
