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    <title>Annulation reactions of heterocyclic chlorovinylaldehydes</title>
    <subTitle>synthesis of functionalized 6H-benzo[c]chromen-6-ones (biaryl lactones), 6H-benzo[c]chromenes and heteroannulated pyridines</subTitle>
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    <namePart>Abbasi, Muhammad Shakeel Ahmed</namePart>
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  <abstract type="Summary">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.</abstract>
  <note type="statement of responsibility">Muhammad Shakeel Ahmed Abbasi</note>
  <note type="thesis">Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2015</note>
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      <title>Annulation reactions of heterocyclic chlorovinylaldehydes</title>
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      <namePart>Abbasi, Muhammad Shakeel Ahmed, 1975 - </namePart>
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