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Anodic Oxidation of Phenols: A Key Step for the Synthesis of Natural Products.
Yamamoto, Takashi; Saitoh, Tsuyoshi; Einaga, Yasuaki; Nishiyama, Shigeru.
  • Yamamoto T; Department of Chemistry, Keio University, 3-14-1 Hiyoshi, Yokohama, 223-8522, Japan.
  • Saitoh T; International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, 1-1-1 Tennodai, Tsukuba, 305-8575, Japan.
  • Einaga Y; Department of Chemistry, Keio University, 3-14-1 Hiyoshi, Yokohama, 223-8522, Japan.
  • Nishiyama S; Department of Chemistry, Keio University, 3-14-1 Hiyoshi, Yokohama, 223-8522, Japan.
Chem Rec ; 21(9): 2254-2268, 2021 Sep.
Article en En | MEDLINE | ID: mdl-33759336
ABSTRACT
Natural products have played a significant role not only in discovery of drugs but also in development of organic chemistry by providing the synthetic challenges. Inspired by biosynthesis where enzymes catalyze a multi-step reaction, we have investigated the natural product synthesis utilizing electrochemical reactions as the key step. Electrochemical organic synthesis, so-called electro-organic synthesis, enables to control the reactivity of substrates simply by tuning electrolysis conditions. In this Personal Account, we overview the recent progress of our research projects about natural product synthesis, in which anodic oxidation of phenol compounds affords the important frameworks such as diaryl ether, spirodienone, and spiroisoxazoline.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenoles / Productos Biológicos Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenoles / Productos Biológicos Idioma: En Año: 2021 Tipo del documento: Article