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Photo- and electro-chemical strategies for the activations of strong chemical bonds.
Tian, Xianhai; Liu, Yuliang; Yakubov, Shahboz; Schütte, Jonathan; Chiba, Shunsuke; Barham, Joshua P.
Afiliação
  • Tian X; Fakultät für Chemie und Pharmazie, Universität Regensburg, 93040 Regensburg, Germany. Joshua-Philip.Barham@chemie.uni-regensburg.de.
  • Liu Y; School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore 637371, Singapore. shunsuke@ntu.edu.sg.
  • Yakubov S; Fakultät für Chemie und Pharmazie, Universität Regensburg, 93040 Regensburg, Germany. Joshua-Philip.Barham@chemie.uni-regensburg.de.
  • Schütte J; Fakultät für Chemie und Pharmazie, Universität Regensburg, 93040 Regensburg, Germany. Joshua-Philip.Barham@chemie.uni-regensburg.de.
  • Chiba S; School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore 637371, Singapore. shunsuke@ntu.edu.sg.
  • Barham JP; Fakultät für Chemie und Pharmazie, Universität Regensburg, 93040 Regensburg, Germany. Joshua-Philip.Barham@chemie.uni-regensburg.de.
Chem Soc Rev ; 53(1): 263-316, 2024 Jan 02.
Article em En | MEDLINE | ID: mdl-38059728
The employment of light and/or electricity - alternatively to conventional thermal energy - unlocks new reactivity paradigms as tools for chemical substrate activations. This leads to the development of new synthetic reactions and a vast expansion of chemical spaces. This review summarizes recent developments in photo- and/or electrochemical activation strategies for the functionalization of strong bonds - particularly carbon-heteroatom (C-X) bonds - via: (1) direct photoexcitation by high energy UV light; (2) activation via photoredox catalysis under irradiation with relatively lower energy UVA or blue light; (3) electrochemical reduction; (4) combination of photocatalysis and electrochemistry. Based on the types of the targeted C-X bonds, various transformations ranging from hydrodefunctionalization to cross-coupling are covered with detailed discussions of their reaction mechanisms.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article