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Application of Metal-Free Dearomatization Reaction as a Sustainable Strategy to Direct Access Complex Cyclic Compounds.
Xu, Xianjun; Zhong, Ling; Feng, Huangdi; Van der Eycken, Erik V.
Afiliação
  • Xu X; Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven, 3001, Belgium.
  • Zhong L; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China.
  • Feng H; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China.
  • Van der Eycken EV; Shanghai Frontiers Science Research Center for Druggability of Cardiovascular Noncoding RNA, Shanghai University of Engineering Science, Shanghai, 201620, China.
Chem Rec ; 23(10): e202300101, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37132130
ABSTRACT
The highly efficient construction of complicated heterocyclic frameworks in an atom- and step-economic manner is still one of the cores of synthetic chemistry. Dearomatization reactions show the unique advantage for the construction of functionalized heterocycles and have attracted widespread attention over the past two decades. The metal-free approach has proved to be a green and sustainable paradigm for the synthesis of spirocyclic, polycyclic and heterocyclic scaffolds, which are widely present in natural products and bioactive molecules. In this review, the advances in the recent six years (2017-2023) in metal-free dearomatization reactions are highlighted. Emphasis is placed on developments in the field of organo-catalyzed dearomatization reactions, oxidative dearomatization reactions, Brønsted acid- or base-promoted dearomatization reactions, photoredox-catalyzed dearomatization reactions, and electrochemical oxidation dearomatization reactions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Rec Assunto da revista: QUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Rec Assunto da revista: QUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica