Photo- and electro-chemical strategies for indazole synthesis

Binbin Huang
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引用次数: 0

Abstract

The indazole core is prevalently found in the structures of bioactive molecules, demonstrating promising potential in medicinal chemistry and drug discovery, which therefore has attracted sustained attention from the synthetic community. Over the recent decades, significant progress has been achieved in both organic photocatalysis and electrosynthesis, offering novel approaches for the efficient and sustainable synthesis of various functionalized indazoles. This mini-review highlights the emerging methodological advancements in photo-/electro-chemical synthesis of two common forms of indazole, namely 1H- and 2H-indazoles, which are classified by specific intramolecular bond formation patterns: (1) C–C bond formation, (2) C–N bond formation, and (3) N–N bond formation. The reaction conditions, representative scopes, and mechanistic understandings of these protocols are emphasized, to elucidate the advantages and limitations in current strategies, with an aim to inspire future innovations that may address challenges in modern indazole synthesis.

Abstract Image

吲哚唑合成的光电化学策略
吲哚唑核普遍存在于生物活性分子的结构中,在药物化学和药物发现方面显示出良好的潜力,因此一直受到合成界的关注。近几十年来,有机光催化和电合成都取得了重大进展,为各种功能化吲哚的高效、可持续合成提供了新的途径。本文重点介绍了光/电化学合成两种常见形式的茚唑的新方法进展,即1H-和2h -茚唑,它们按特定的分子内键形成模式分类:(1)C-C键形成,(2)C-N键形成,(3)N-N键形成。强调了这些方案的反应条件,代表性范围和机理理解,以阐明当前策略的优点和局限性,目的是激发未来可能解决现代吲哚合成挑战的创新。
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来源期刊
Tetrahedron chem
Tetrahedron chem Organic Chemistry
CiteScore
3.60
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审稿时长
27 days
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