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Rhodium-Catalyzed Regioselective C7-Functionalization of N-Pivaloylindoles.
Xu, Lanting; Zhang, Chao; He, Yupeng; Tan, Lushi; Ma, Dawei.
Afiliação
  • Xu L; State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China).
  • Zhang C; Liaoning Shihua University, Dandong Lu West 1, Fushun 113001 (China).
  • He Y; Liaoning Shihua University, Dandong Lu West 1, Fushun 113001 (China).
  • Tan L; Merck Research Laboratories, P.O. Box 2000, RY800-D280, Rahway, NJ 07065-0900 (USA). lushi_tan@merck.com.
  • Ma D; State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China). madw@mail.sioc.ac.cn.
Angew Chem Int Ed Engl ; 55(1): 321-5, 2016 Jan 04.
Article em En | MEDLINE | ID: mdl-26510833
An efficient rhodium-catalyzed method for direct C-H functionalization at the C7 position of a wide range of indoles has been developed. Good to excellent yields of alkenylation products were observed with acrylates, styrenes, and vinyl phenyl sulfones, whereas the saturated alkylation products were obtained in good yield with α,ß-unsaturated ketones. Both the N-pivaloyl directing group and the rhodium catalyst proved to be crucial for high regioselectivity and conversion.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2016 Tipo de documento: Article