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
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