Formylation and Bromination of Pyrrolo[2,1-


Journal

The Journal of organic chemistry
ISSN: 1520-6904
Titre abrégé: J Org Chem
Pays: United States
ID NLM: 2985193R

Informations de publication

Date de publication:
06 Aug 2021
Historique:
pubmed: 3 7 2021
medline: 3 7 2021
entrez: 2 7 2021
Statut: ppublish

Résumé

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%).

Identifiants

pubmed: 34213904
doi: 10.1021/acs.joc.1c00844
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10118-10128

Auteurs

Jia-Qin Li (JQ)

Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.

Hui-Lin Tan (HL)

Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.

Dan-Dan Ma (DD)

Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.

Xin-Xin Zhu (XX)

Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.

Hai-Lei Cui (HL)

Laboratory of Asymmetric Synthesis, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, P.R. China.

Classifications MeSH