Access to Thienopyridine and Thienoquinoline Derivatives via Site-Selective C-H Bond Functionalization and Annulation.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
06 05 2022
Historique:
pubmed: 26 4 2022
medline: 10 5 2022
entrez: 25 4 2022
Statut: ppublish

Résumé

To develop of an effective synthetic methodology for biologically relevant thienopyridines, a concise and efficient protocol is described for the synthesis of a series of substituted thienopyridine and thienoquinoline derivatives with high selectivity using EtOCS

Identifiants

pubmed: 35467892
doi: 10.1021/acs.orglett.2c00903
doi:

Substances chimiques

Pyridines 0
Thienopyridines 0
thienopyridine 0
Sulfur 70FD1KFU70

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3167-3172

Auteurs

Runfa He (R)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

Yang Liu (Y)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

Yingqi Feng (Y)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

Lu Chen (L)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

Yubing Huang (Y)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

Feng Xie (F)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

Yibiao Li (Y)

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529090, China.

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Classifications MeSH