Progress on the Synthesis and Applications of Aminals: Scaffolds for Molecular Diversity

Synthesis Pub Date : 2024-06-10 DOI:10.1055/a-2317-6604
Rafael Rippel, Luísa M. Ferreira, Paula S. Branco
{"title":"Progress on the Synthesis and Applications of Aminals: Scaffolds for Molecular Diversity","authors":"Rafael Rippel, Luísa M. Ferreira, Paula S. Branco","doi":"10.1055/a-2317-6604","DOIUrl":null,"url":null,"abstract":"<p>Aminals, characterized by a central carbon linking two nitrogen atoms, are versatile building blocks in modern chemistry. This review addresses a literature gap by exploring the synthesis and applications of aminals, with a focus on drug discovery and molecular diversity. Beyond medicinal chemistry, aminals find applications as key components in bioactive compounds and as versatile tools in materials chemistry. The review covers fundamental characteristics, synthetic methodologies, stability, and applications, emphasizing alternative synthetic methods to the well-established aldehyde–amine condensation. This inclusive exploration provides insights into diverse synthetic pathways that expand the versatility of the aminal scaffold.</p> <p>1 Introduction</p> <p>2 The Aminal Group</p> <p>3 Aminal Synthesis</p> <p>3.1 Metal-Free Approaches</p> <p>3.2 Metal-Catalyzed Approaches</p> <p>3.3 Photoredox Methodologies</p> <p>3.4 Via Rearrangements</p> <p>3.5 Via Decarboxylative Coupling</p> <p>4 Aminals as Synthetic Tools</p> <p>5 Synthesis of Aminal-Containing Natural Products</p> <p>6 Aminal-Based Materials</p> <p>7 Conclusions</p> ","PeriodicalId":501298,"journal":{"name":"Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-10","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/a-2317-6604","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Aminals, characterized by a central carbon linking two nitrogen atoms, are versatile building blocks in modern chemistry. This review addresses a literature gap by exploring the synthesis and applications of aminals, with a focus on drug discovery and molecular diversity. Beyond medicinal chemistry, aminals find applications as key components in bioactive compounds and as versatile tools in materials chemistry. The review covers fundamental characteristics, synthetic methodologies, stability, and applications, emphasizing alternative synthetic methods to the well-established aldehyde–amine condensation. This inclusive exploration provides insights into diverse synthetic pathways that expand the versatility of the aminal scaffold.

1 Introduction

2 The Aminal Group

3 Aminal Synthesis

3.1 Metal-Free Approaches

3.2 Metal-Catalyzed Approaches

3.3 Photoredox Methodologies

3.4 Via Rearrangements

3.5 Via Decarboxylative Coupling

4 Aminals as Synthetic Tools

5 Synthesis of Aminal-Containing Natural Products

6 Aminal-Based Materials

7 Conclusions

Abstract Image

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
Aminals 的合成和应用进展:分子多样性的支架
氨基化合物的特点是一个中心碳连接两个氮原子,是现代化学中用途广泛的构筑基块。本综述通过探讨氨基化合物的合成和应用,填补了文献空白,重点关注药物发现和分子多样性。除药物化学外,氨基化合物还可作为生物活性化合物的关键成分和材料化学的多功能工具加以应用。这篇综述涵盖了基本特征、合成方法、稳定性和应用,并强调了除成熟的醛胺缩合之外的其他合成方法。这种包容性的探索为我们提供了对各种合成途径的深入了解,从而拓展了氨基化合物支架的多功能性。1 引言 2 氨基醛基 3 氨基醛合成 3.1 无金属方法 3.2 金属催化方法 3.3 光氧化方法 3.4 通过重排 3.5 通过脱羧偶联 4 氨基醛作为合成工具 5 含氨基醛天然产物的合成 6 氨基醛基材料 7 结论
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 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