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Synthesis of [1,2,3]Triazolo-[1,5-a]quinoxalin-4(5H)-ones through Photoredox-Catalyzed [3 + 2] Cyclization Reactions with Hypervalent Iodine(III) Reagents.
Wen, Jinxia; Zhao, Wenyan; Gao, Xu; Ren, Xiaofang; Dong, Chunping; Wang, Cheli; Liu, Li; Li, Jian.
Afiliación
  • Wen J; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Zhao W; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Gao X; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Ren X; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Dong C; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Wang C; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Liu L; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
  • Li J; School of Pharmacy, Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Changzhou, 213164, China.
J Org Chem ; 87(6): 4415-4423, 2022 Mar 18.
Article en En | MEDLINE | ID: mdl-35234036
ABSTRACT
An efficient synthesis of a variety of [1,2,3]triazolo-[1,5-a]quinoxalin-4(5H)-ones via a [3 + 2] cyclization reaction by photoredox catalysis between quinoxalinones and hypervalent iodine(III) reagents is reported. A range of quinoxalinones and hypervalent iodine(III) reagents were tolerated well. This cyclization reaction allows access to structurally diverse [1,2,3]triazolo-[1,5-a]quinoxalin-4(5H)-ones in moderate to good yields.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2022 Tipo del documento: Article País de afiliación: China