4.8 Article

Chemoselective N-Heterocyclic Carbene-Catalyzed Cross-Benzoin Reactions: Importance of the Fused Ring in Triazolium Salts

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 21, 页码 7539-7542

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AMER CHEMICAL SOC
DOI: 10.1021/ja501772m

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  1. Government of Saskatchewan for an Innovation and Opportunity Scholarship
  2. Natural Sciences and Engineering Research Council of Canada
  3. Canada Foundation for Innovation
  4. University of Saskatchewan

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Morpholinone- and piperidinone-derived triazolium salts are shown to catalyze highly chemoselective cross-benzoin reactions between aliphatic and aromatic aldehydes. The reaction scope includes ortho-, tneta-, and para-substituted benzaldehyde derivatives with a range of electron-donating and -withdrawing groups as well as branched and unbranched aliphatic aldehydes. Catalytic loadings as low as 5 mol % give excellent yields in these reactions (up to 99%).

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