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        Synfacts  2010(2): 0142-0142  
DOI: 10.1055/s-0029-1219029
   DOI: 10.1055/s-0029-1219029
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag
      Stuttgart ˙ New YorkFormal Synthesis of (+)-Indatraline
K. Yoo, H. Kim, J. Yun*
Sungkyunkwan University, Suwon, Korea
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   Publikationsverlauf
Publikationsdatum:
21. Januar 2010 (online)
Significance
The key step in this formal synthesis of (+)-indatraline is a catalytic asymmetric conjugate reduction (B → C) of a β,β-diaryl-α,β-unsaturated nitrile using copper hydride coordinated to (R)-Josiphos. Further 11 examples are reported (78-91% yield) with typical ee values exceeding 90% even in cases where the two aryl groups have a similar steric demand.