4.7 Article

Enantioselective monofluoromethylation of aldehydes with 2-fluoro-1,3-benzodithiole-1,1,3,3-tetraoxide catalyzed by a bifunctional cinchona alkaloid-derived thiourea-titanium complex

Journal

CHEMICAL COMMUNICATIONS
Volume 49, Issue 95, Pages 11206-11208

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc46544f

Keywords

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Funding

  1. Platform for Drug Discovery, Informatics, and Structural Life Science from the Ministry of Education, Culture, Sports, Science and Technology, Japan
  2. MEXT (Ministry of Education, Culture, Sports, Science and Technology) [24105513, 2304]
  3. JST (ACT-C: Creation of Advanced Catalytic Transformation for the Sustainable Manufacturing at Low Energy, Low Environmental Load)
  4. Grants-in-Aid for Scientific Research [24655048] Funding Source: KAKEN

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A catalytic enantioselective monofluoromethylation of aldehydes using 2-fluoro-1,3-benzodithiole-1,1,3,3-tetraoxide (FBDT) was realized. With a bifunctional thiourea-titanium catalytic system, the monofluoromethylated- adducts were obtained in good yields and high enantioselectivities, up to 96% ee.

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