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

期刊

CHEMICAL COMMUNICATIONS
卷 49, 期 95, 页码 11206-11208

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc46544f

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资金

  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

向作者/读者索取更多资源

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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