4.7 Article

Highly enantioselective copper(I)-catalyzed conjugate addition of 1,3-diynes to α,β-unsaturated trifluoromethyl ketones

Journal

CHEMICAL COMMUNICATIONS
Volume 51, Issue 43, Pages 8958-8961

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc01676b

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Funding

  1. Ministerio de Economia y Competitividad (MINECO-Gobierno de Espana)
  2. FEDER (EU) [CTQ2013-47494-P]
  3. Generalitat Valenciana [ISIC2012/001]
  4. MINECO

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The conjugate diynylation of alpha,beta-unsaturated trifluoromethyl ketones is carried out in the presence of a low catalytic load (2.5 mol%) of a copper(I)-MeOBIPHEP complex, triethylamine and a terminal 1,3-diyne. Pre-metalation of the terminal 1,3-diyne with stoichiometric or higher amounts of dialkylzinc reagent is not required. The corresponding internal diynes bearing a propargylic stereogenic center are obtained with good yields and excellent enantioselectivities.

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