4.8 Article

Iridium-Catalyzed Enantioselective Allyl-Alkene Coupling

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 8, Pages 3006-3009

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja412962w

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Funding

  1. ETH Zurich
  2. Swiss National Science Foundation

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The direct Ir-catalyzed cross-coupling between branched, racemic allylic alcohols and simple olefins is described. This transformation is catalyzed by an Ir-(P,olefin) complex and proceeds with high site selectivity and excellent enantioselectivity. The method allows rapid access to various 1,5-dienes or trienes and was used in the catalytic asymmetric synthesis of the gamma-secretase modulator JNJ-40418677.

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