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Metal-Free Synthesis of 2H-Indazole Skeletons by Photochemistry or Thermochemistry.
Zhang, Gan; Zhang, Yicheng; Li, Pinhua; Zhou, Chao; Wang, Min; Wang, Lei.
Afiliação
  • Zhang G; Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education and Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.
  • Zhang Y; Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education and Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.
  • Li P; Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education and Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.
  • Zhou C; Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education and Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.
  • Wang M; Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education and Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.
  • Wang L; Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education and Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China.
J Org Chem ; 88(17): 12341-12356, 2023 Sep 01.
Article em En | MEDLINE | ID: mdl-37582245
ABSTRACT
A simple and tuned synthesis of a 2H-indazole skeleton under metal-free conditions was developed. Under visible-light irradiation at room temperature, 2-((aryl/alkyl/H)ethynyl))aryltriazenes reacted with arylsulfinic acids to afford 3-functionalized 2H-indazoles without extra photocatalyst via an electron donor-acceptor complex. In the presence of arylsulfinic acid, 2-(ethynyl)aryltriazenes underwent an intramolecular oxidation/cyclization to provide 2H-indazole-3-carbaldehydes at 50 °C in air.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article