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Base-Promoted Synthesis of Isoquinolines through a Tandem Reaction of 2-Methyl-arylaldehydes and Nitriles.
Shuai, Sujuan; Mao, Jianyou; Zhou, Fan; Yan, Qifeng; Chen, Lingfeng; Li, Jie; Walsh, Patrick J; Liang, Guang.
Afiliação
  • Shuai S; School of Pharmaceutical Sciences, Hangzhou Medical College, Hangzhou, Zhejiang 311399, China.
  • Mao J; Department of Pharmacy, School of Medicine, Zhejiang University City College, No. 48, Huzhou Road, Hangzhou 310015, P. R. China.
  • Zhou F; College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, P. R. China.
  • Yan Q; Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Jiangsu National Synergetic Innovation Center for Advanced Materials, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, P. R. China.
  • Chen L; School of Pharmaceutical Sciences, Hangzhou Medical College, Hangzhou, Zhejiang 311399, China.
  • Li J; Department of Pharmacy, School of Medicine, Zhejiang University City College, No. 48, Huzhou Road, Hangzhou 310015, P. R. China.
  • Walsh PJ; College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, P. R. China.
  • Liang G; School of Pharmaceutical Sciences, Hangzhou Medical College, Hangzhou, Zhejiang 311399, China.
J Org Chem ; 89(10): 6793-6797, 2024 May 17.
Article em En | MEDLINE | ID: mdl-38691096
ABSTRACT
A convenient method for preparing 3-aryl isoquinolines via a base-promoted tandem reaction is presented. Simply combining commercially available 2-methyl-arylaldehydes, benzonitriles, NaN(SiMe3)2, and Cs2CO3 enabled the synthesis of a variety of isoquinolines (23 examples, ≤90% yield). Among the syntheses of isoquinolines, the transition metal-free method described here is straightforward, practical, and operationally simple.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article