Recent Advances in the Reactions of β-Naphthol at α-Position

  • Jing Liu ,
  • Jintao Chen ,
  • Tingting Liu ,
  • Jia Liu ,
  • Yaofu Zeng
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  • School of Pharmaceutical Science, Hengyang Medical School, University of South China, Hengyang, Hunan 421000
†(These authors contributed equally to this work).
* Corresponding author.

Received date: 2022-07-07

  Revised date: 2022-08-22

  Online published: 2022-10-14

Supported by

Undergraduate Training Programs for Innovative and Entrepreneurship in Hunan Province(S202210555288); Undergraduate Training Programs for Innovative and Entrepreneurship in Hunan Province(S202110555254); Innovation and Entrepreneurship for College Students of University of South China(X202210555181)

Abstract

β-Naphthol is an important synthon in organic synthesis and can participate in various chemical reactions due to its active chemical property at α-site, which has attracted a great attention from chemists. β-Naphthol can undergo various chemical transformations at α-position, such as alkylation, arylation, cyclization, amination, halogenation and so on, which can be used to construct structurally diverse naphthol derivatives with various biological activities. These naphthol derivatives can be used not only as the privileged skeletons of natural active drugs, but also as the building blocks for the preparation of the important intermediates in chemical synthesis. In recent years, chemical reactions based on β-naphthol at α-site have emerged one after another. The reactions of β-naphthol at α-position are reviewed from the aspects of C-C, C-N, C-O, C-X, C-S, C-P bond constructions and so on.

Cite this article

Jing Liu , Jintao Chen , Tingting Liu , Jia Liu , Yaofu Zeng . Recent Advances in the Reactions of β-Naphthol at α-Position[J]. Chinese Journal of Organic Chemistry, 2023 , 43(2) : 379 -410 . DOI: 10.6023/cjoc202207015

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