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        Synlett 1992; 1992(4): 354-356
DOI: 10.1055/s-1992-22013
   DOI: 10.1055/s-1992-22013
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany.  All rights reserved.
      This journal, including all individual contributions and  illustrations published
      therein, is legally protected by copyright for the duration of  the copyright period.
      Any use, exploitation or commercialization outside the narrow  limits set by copyright
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      data processing and storage.A Novel Synthesis of Hemispherands
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   Publikationsverlauf
Publikationsdatum:
08. März 2002 (online)
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A novel, flexible synthesis of hemispherands {2,5,8-trioxa[9](3,3″) m-terphenylophanes 5a-d} with different central aromatic groups is described. The key step comprises the introduction of the central aromatic ring in the last step of the synthesis via a Suzuki cross-coupling reaction using palladium tetrakis(triplienylphosphine) as a catalyst and sodium or potassium cations serving as a template ion in the macrocyclization.
 
    