Dynamic Kinetic Resolution-Enabled Highly Stereoselective Nucleophilic Fluoroalkylation to Access Chiral ß-Fluoro Amines.

Liu, Qinghe; Kong, Taige; Ni, Chuanfa; Hu, Jinbo

Liu, Qinghe; Kong, Taige; Ni, Chuanfa; Hu, Jinbo.

Afiliación

Liu Q; Key Laboratory of Organofluorine Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai 200032, P. R. China.
Kong T; Key Laboratory of Organofluorine Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai 200032, P. R. China.
Ni C; Key Laboratory of Organofluorine Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai 200032, P. R. China.
Hu J; Key Laboratory of Organofluorine Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai 200032, P. R. China.

Org Lett ; 24(32): 5982-5987, 2022 08 19.

Article en En | MEDLINE | ID: mdl-35939038

Asunto(s)

Aminas; Iminas; Aminas/química; Aniones/química; Iminas/química; Cinética; Estereoisomerismo

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Aminas / Iminas Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article

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