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Selectfluor Mediated Direct C-H Fluorination of 3-Heteroaryl-Oxindoles.
Qin, Hui; Wei, Guo-Liang; Zheng, Xiao-Wei; Zhang, Yi-Wen; Huang, Ping.
Afiliação
  • Qin H; Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang 310014, China.
  • Wei GL; Key Laboratory of Endocrine Gland Diseases of Zhejiang Province, Hangzhou, Zhejiang 310014, China.
  • Zheng XW; Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang 310014, China.
  • Zhang YW; Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang 310014, China.
  • Huang P; Key Laboratory of Endocrine Gland Diseases of Zhejiang Province, Hangzhou, Zhejiang 310014, China.
J Org Chem ; 89(1): 740-747, 2024 Jan 05.
Article em En | MEDLINE | ID: mdl-38101804
ABSTRACT
An efficient transition-metal-free fluorination synthesis of N-H-free 3-heteroaryl-oxindoles with Selectfluor was depicted. Under mild reaction conditions, a series of 3-heteroaryl-fluorooxindoles were produced in yield of 62-88% using Selectfluor as a fluorine source.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2024 Tipo de documento: Article