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Formylation and Bromination of Pyrrolo[2,1-a]isoquinoline Derivatives with Bromoisobutyrate and Dimethyl Sulfoxide.
Li, Jia-Qin; Tan, Hui-Lin; Ma, Dan-Dan; Zhu, Xin-Xin; Cui, Hai-Lei.
Afiliação
  • Li JQ; Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.
  • Tan HL; Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.
  • Ma DD; Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.
  • Zhu XX; Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.
  • Cui HL; Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.
J Org Chem ; 86(15): 10118-10128, 2021 Aug 06.
Article em En | MEDLINE | ID: mdl-34213904
We have developed an efficient formylation of pyrroloisoquinolines using bromoisobutyrate and dimethyl sulfoxide as carbonyl reagent. Various formylated pyrroloisoquinolines could be prepared in good yields (up to 94%). This formylation process can be easily scaled up to gram scale with good yield. In most cases of pyrroloisoquinolines without methoxy groups, the combination of bromoisobutyrate and dimethyl sulfoxide could act as a bromination reagent, delivering brominated pyrroloisoquinolines in acceptable to good yields (up to 82%).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article