Recent advances in copper-catalyzed multicomponent reactions with photoinduction

Copper-catalyzed multicomponent reactions (MCRs) have garnered growing attention from synthetic chemists, due to their compelling attributes, such as cost-effectiveness, low toxicity, versatility in orchestrating one or two-electron processes, and the extraordinary capacity to enhance molecular complexity in a single step. The synergistic combination of these reactions with photocatalysis paves the way for novel reaction pathways, offering opportunities for new transformations executed under gentler, more environmentally-friendly conditions. Copper's catalytic prowess is further underscored by its adept management of key intermediate stability and reactivity within photochemical frameworks, a testament to its multifaceted utility. Furthermore, the strategic introduction of suitable chiral ligands enables photoinduced copper-catalyzed asymmetric MCRs, streamlining the synthesis of a variety of new chiral compounds in an atom- and step-economical manner. This review aims to comprehensively encapsulate the recent advancements in photoinduced copper-catalyzed MCRs, including racemic and asymmetric fashions, dissecting the underlying reaction mechanisms, and charting a course for future explorations in this promising field. © 2025 Elsevier B.V., All rights reserved.

Авторы
Song Liangliang 1 , Cai Lingchao 1 , Van Der Eycken Erik V. 2, 3 , Gong Lei 4, 5
Издательство
Elsevier Science Publishing Company, Inc.
Язык
Английский
Статус
Опубликовано
Номер
216428
Том
528
Год
2025
Организации
  • 1 College of Chemical Engineering, Nanjing Forestry University, Nanjing, China
  • 2 Department of Chemistry, KU Leuven, Leuven, Belgium
  • 3 RUDN University, Moscow, Russian Federation
  • 4 College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, China
  • 5 School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, China
Ключевые слова
Asymmetric catalysis; Copper; Multicomponent reaction; Photocatalysis; Radical
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