Chiral Indoline-2-carboxylic Acid Enables Highly Enantioselective Catellani-type Annulation with 4-(Bromomethyl)cyclohexanone.

Chen, Xin-Meng; Zhu, Ling; Chen, Dian-Feng; Gong, Liu-Zhu

Chen, Xin-Meng; Zhu, Ling; Chen, Dian-Feng; Gong, Liu-Zhu.

Afiliação

Chen XM; Hefei National Laboratory for Physical Sciences at the Microscale, and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, China.
Zhu L; Hefei National Laboratory for Physical Sciences at the Microscale, and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, China.
Chen DF; Hefei National Laboratory for Physical Sciences at the Microscale, and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, China.
Gong LZ; Hefei National Laboratory for Physical Sciences at the Microscale, and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, China.

Angew Chem Int Ed Engl ; 60(47): 24844-24848, 2021 11 15.

Article em En | MEDLINE | ID: mdl-34519147

Palavras-chave

C−H activation; asymmetric Catellani annulation; chiral amines; cooperative catalysis; palladium

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

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