Consecutive Intermolecular Reductive Amination/Asymmetric Hydrogenation: Facile Access to Sterically Tunable Chiral Vicinal Diamines and N-Heterocyclic Carbenes.

Chen, Ya; Pan, Yixiao; He, Yan-Mei; Fan, Qing-Hua

Chen, Ya; Pan, Yixiao; He, Yan-Mei; Fan, Qing-Hua.

Afiliação

Chen Y; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences (ICCAS), University of Chinese Academy of Sciences, Beijing, 100190, P. R. China.
Pan Y; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences (ICCAS), University of Chinese Academy of Sciences, Beijing, 100190, P. R. China.
He YM; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences (ICCAS), University of Chinese Academy of Sciences, Beijing, 100190, P. R. China.
Fan QH; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences (ICCAS), University of Chinese Academy of Sciences, Beijing, 100190, P. R. China.

Angew Chem Int Ed Engl ; 58(47): 16831-16834, 2019 Nov 18.

Article em En | MEDLINE | ID: mdl-31486574

Palavras-chave

N-heterocyclic carbenes; asymmetric hydrogenation; reductive amination; tandem reactions; vicinal diamines

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2019 Tipo de documento: Article

Texto completo

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2019 Tipo de documento: Article