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
{"title":"光诱导迷你型反应的研究进展","authors":"Mario Martos, Irene Bosque, Jose C. Gonzalez-Gomez","doi":"10.1055/s-0043-1775387","DOIUrl":null,"url":null,"abstract":"<p>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.</p> <p>1 Introduction</p> <p>2 Using Noble-Metal-Based Photocatalysts</p> <p>3 Noble-Metal-Free Methods Using Sacrificial Oxidants</p> <p>4 Noble-Metal-Free Methods Without Sacrificial Oxidants</p> <p>5 Conclusions and Perspectives</p> ","PeriodicalId":501298,"journal":{"name":"Synthesis","volume":"78 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Advances in Photoinduced Minisci-like Reactions\",\"authors\":\"Mario Martos, Irene Bosque, Jose C. Gonzalez-Gomez\",\"doi\":\"10.1055/s-0043-1775387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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.</p> <p>1 Introduction</p> <p>2 Using Noble-Metal-Based Photocatalysts</p> <p>3 Noble-Metal-Free Methods Using Sacrificial Oxidants</p> <p>4 Noble-Metal-Free Methods Without Sacrificial Oxidants</p> <p>5 Conclusions and Perspectives</p> \",\"PeriodicalId\":501298,\"journal\":{\"name\":\"Synthesis\",\"volume\":\"78 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/s-0043-1775387\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-0043-1775387","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Facile Synthesis of Silanols via Cesium Carbonate Catalyzed Hydrosilanes with Water Discovery Process Chemistry: An Innovation Hub at the Interface of Academia, the Pharmaceutical Industry, and Contract Research Organization Accessing a Medicinal-Chemistry-Relevant Chemical Space with sp2–sp3 Hybrid Heterocyclic Fragments Recent Advances in Diazophosphonate Chemistry: Reactions and Transformations Recent Advances in Fluoroalkylation Strategies: Exploring Novel Reactivities and Synthetic Applications of Sulfone- and Sulfinate-Based Reagents for Mono-, Di-, and Trifluoromethylations
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1