Silver-Catalyzed Reduction of Quinolines in Water.

Wang, Yan; Dong, Baobiao; Wang, Zikun; Cong, Xuefeng; Bi, Xihe

Wang, Yan; Dong, Baobiao; Wang, Zikun; Cong, Xuefeng; Bi, Xihe.

Afiliação

Wang Y; School of Chemistry and Life Science , Changchun University of Technology , Changchun 130012 , China.
Dong B; Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry , Northeast Normal University , Changchun 130024 , China.
Wang Z; Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry , Northeast Normal University , Changchun 130024 , China.
Cong X; Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry , Northeast Normal University , Changchun 130024 , China.
Bi X; Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry , Northeast Normal University , Changchun 130024 , China.

Org Lett ; 21(10): 3631-3634, 2019 05 17.

Article em En | MEDLINE | ID: mdl-31062984

ABSTRACT

ABSTRACT

A ligand- and base-free silver-catalyzed reduction of quinolines and electron-deficient aromatic N-heteroarenes in water has been described. Mechanistic studies revealed that the effective reducing species was Ag-H. This versatile catalytic protocol provided facile, environmentally friendly, and practical access to a variety of 1,2,3,4-tetrahydroquinoline derivatives at room temperature.

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

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