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Photoredox/Nickel Dual Catalysis-Enabled Aryl Formylation with 2,2-Dimethoxy-N,N-dimethylethan-1-amine as CO Source.
Gao, Jie; He, Xian-Chen; Liu, Yan-Ling; Yao, Pin-Pin; Guan, Jian-Ping; Chen, Kai; Xiang, Hao-Yue; Yang, Hua.
Affiliation
  • Gao J; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • He XC; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Liu YL; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Yao PP; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Guan JP; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Chen K; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Xiang HY; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Yang H; School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, Henan P. R. China.
Org Lett ; 26(7): 1478-1482, 2024 Feb 23.
Article de En | MEDLINE | ID: mdl-38334422
ABSTRACT
Herein, a dual photoredox/nickel catalyzed formylation of aryl bromide with commercially available 2,2-dimethoxy-N,N-dimethylethan-1-amine as an effective CO source has been successfully achieved, delivering a series of aromatic aldehydes in moderate to good yields. Compared with the traditional reductive carbonylation process, this newly designed synthetic protocol provides a straightforward toolbox to access aromatic aldehydes, obviating the use of carbon monoxide and stoichiometric reductants. Finally, the utility of this direct formylation reaction was demonstrated in the pharmaceutical analogue synthesis.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Lett Sujet du journal: BIOQUIMICA Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Lett Sujet du journal: BIOQUIMICA Année: 2024 Type de document: Article