光诱导迷你型反应的研究进展

Synthesis Pub Date : 2024-07-29 DOI:10.1055/s-0043-1775387
Mario Martos, Irene Bosque, Jose C. Gonzalez-Gomez
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引用次数: 0

摘要

Minisci 反应已有五十多年的历史,目前仍是直接烷基化碱性杂环戊烯的首选工具。最近光催化技术的发展为在更温和、更可持续的条件下生成自由基开辟了新的途径。将这种方法应用到 Minisci 反应中重新激发了人们对这种转化的兴趣,而这种转化本身在药物化学中就具有吸引力。应仔细研究牺牲氧化剂、催化剂和特定反应条件等方面,以评估该方案的实用性。本简短综述重点介绍光诱导 Minisci- 型反应的最新进展(2020 年至 2024 年 2 月),强调可持续性。1 引言 2 使用贵金属光催化剂 3 使用人工合成氧化剂的无贵金属方法 4 无人工合成氧化剂的无贵金属方法 5 结论与展望
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Advances in Photoinduced Minisci-like Reactions

Advances in Photoinduced Minisci-like Reactions

The Minisci reaction, which has been around for more than five decades, is still the preferred tool for the straightforward alkylation of basic heteroarenes. The recent developments in photocatalysis have opened novel pathways for radical generation under milder and more sustainable conditions. Implementing this approach into the Minisci reaction has renewed interest in this transformation, which is attractive per se in Medicinal Chemistry. Aspects such as sacrificial oxidants, catalysts, and specific reaction conditions should be carefully examined to evaluate the practicability of the protocol. This short review focuses on recent advances (2020 to February 2024) in photoinduced Minisci-type reactions, emphasizing sustainability.

1 Introduction

2 Using Noble-Metal-Based Photocatalysts

3 Noble-Metal-Free Methods Using Sacrificial Oxidants

4 Noble-Metal-Free Methods Without Sacrificial Oxidants

5 Conclusions and Perspectives

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