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Metal- and light-free decarboxylative direct C-H alkylation of heteroarenes at room temperature.
Zhang, Tong-Bo; Guan, Xi-Dong; Gao, Yan; Lu, Shi-Chao; Li, Bing-Long.
  • Zhang TB; Harbin Zhenbao Pharmaceutical Co., Ltd, No. 8 First Yantai Road, Jizhong District, Haping Road, Development Zone Harbin, Heilongjiang 150060/CN, P. R. China.
  • Guan XD; National Key Laboratory of Advanced Drug Delivery and Release Systems, School of Pharmaceutical Sciences & Institute of Materia Medica, Shandong First Medical University & Shandong Academy of Medical Sciences, 6699 Qingdao Road, Jinan 250117, P. R. China.
  • Gao Y; College of Biological and Chemical Engineering, Qilu Institute of Technology, Jinan 250200, P. R. China.
  • Lu SC; State Key Laboratory of Bioactive Substance and Function of Natural Medicines and Beijing Key Laboratory of Active Substance Discovery and Druggability Evaluation, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Xicheng District, P. R. China. lushic
  • Li BL; State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, 100191, P. R. China.
Org Biomol Chem ; 22(17): 3439-3443, 2024 May 01.
Article en En | MEDLINE | ID: mdl-38591416
ABSTRACT
This study reports a metal- and light-free decarboxylative C-H alkylation of heteroarenes at room temperature. The reaction generates various primary, secondary, and tertiary alkyl radicals and functionalizes seven different privileged scaffolds widely present in bioactive molecules. During this process, one equivalent of hypervalent iodine(III) carboxylates (HICs) plays dual roles as an alkyl radical precursor and an oxidant.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article