Pyrrolo[2,1-a]isoquinolines as multitasking organophotocatalysts in chemical synthesis

Yuliang Liu, Haoyu Li, Eugene Yew Kun Tan, Erik Budi Santiko, Youhei Chitose, Manabu Abe, Shunsuke Chiba

研究成果: ジャーナルへの寄稿学術誌査読

1 被引用数 (Scopus)

抄録

We demonstrate the design and synthesis of pyrrolo[2,1-a]isoquinolines (PIqs) bearing electron-withdrawing groups, which are excited under irradiation with visible light to display wider redox windows and higher triplet-state energies. The photophysical and electrochemical characters of PIqs can be tailored by modification of the electron-withdrawing groups and their positions, enabling redox-neutral (hetero)biaryl cross-coupling between aryl halides and (hetero)arenes, nickel-catalyzed amination and oxygenation of aryl halides, and decarboxylative cross-coupling between α-amino acids and aryl halides, as well as a set of molecular transformations driven by triplet-triplet sensitization under irradiation with visible light.

本文言語英語
ページ(範囲)2726-2749
ページ数24
ジャーナルChem Catalysis
2
10
DOI
出版ステータス出版済み - 10月 20 2022
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 化学(その他)
  • 物理化学および理論化学
  • 有機化学

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