Highly Enantioselective Synthesis of N-Unprotected Unnatural &#945;-Amino Acid Derivatives by Ruthenium-Catalyzed Direct Asymmetric Reductive Amination.

Hu, Le'an; Wang, Yuan-Zheng; Xu, Lei; Yin, Qin; Zhang, Xumu

Highly Enantioselective Synthesis of N-Unprotected Unnatural α-Amino Acid Derivatives by Ruthenium-Catalyzed Direct Asymmetric Reductive Amination.

Hu, Le'an; Wang, Yuan-Zheng; Xu, Lei; Yin, Qin; Zhang, Xumu.

Afiliación

Hu L; Guangdong Provincial Key Laboratory of Catalysis, Department of Chemistry, Southern University of Science and Technology, Shenzhen, Guangdong 518055, P. R. China.
Wang YZ; Medi-X Pingshan, Southern University of Science and Technology, Shenzhen, Guangdong 518055, P. R. China.
Xu L; Guangdong Provincial Key Laboratory of Catalysis, Department of Chemistry, Southern University of Science and Technology, Shenzhen, Guangdong 518055, P. R. China.
Yin Q; Medi-X Pingshan, Southern University of Science and Technology, Shenzhen, Guangdong 518055, P. R. China.
Zhang X; Shenzhen Institute of Advanced Technology, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shenzhen, Guangdong 518055, P. R. China.

Angew Chem Int Ed Engl ; 61(25): e202202552, 2022 06 20.

Article en En | MEDLINE | ID: mdl-35332974

Asunto(s)

Rutenio; Aminación; Aminoácidos/química; Catálisis; Estereoisomerismo

Palabras clave

Amino Acids; N-Unprotected Amino Acids; Reductive Amination; Ruthenium; α-Keto Amides

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rutenio Idioma: En Revista: Angew Chem Int Ed Engl Año: 2022 Tipo del documento: Article

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