化学
表面改性
分子内力
氢原子
烷氧基
光化学
直接的
反应性(心理学)
激进的
立体化学
有机化学
激发态
烷基
单重态
替代医学
核物理学
物理化学
病理
物理
医学
作者
David A. Nagib,Leah M. Stateman,Kohki M. Nakafuku
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2018-02-12
卷期号:50 (08): 1569-1586
被引量:409
标识
DOI:10.1055/s-0036-1591930
摘要
The selective functionalization of remote C–H bonds via intramolecular hydrogen atom transfer (HAT) is transformative for organic synthesis. This radical-mediated strategy provides access to novel reactivity that is complementary to closed-shell pathways. As modern methods for mild generation of radicals are continually developed, inherent selectivity paradigms of HAT mechanisms offer unparalleled opportunities for developing new strategies for C–H functionalization. This review outlines the history, recent advances, and mechanistic underpinnings of intramolecular HAT as a guide to addressing ongoing challenges in this arena. 1 Introduction 2 Nitrogen-Centered Radicals 2.1 sp3 N-Radical Initiation 2.2 sp2 N-Radical Initiation 3 Oxygen-Centered Radicals 3.1 Carbonyl Diradical Initiation 3.2 Alkoxy Radical Initiation 3.3 Non-alkoxy Radical Initiation 4 Carbon-Centered Radicals 4.1 sp2 C-Radical Initiation 4.2 sp3 C-Radical Initiation 5 Conclusion
科研通智能强力驱动
Strongly Powered by AbleSci AI