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DOI: 10.1055/s-0036-1591930
Remote C–H Functionalization via Selective Hydrogen Atom Transfer
We thank the National Institutes of Health (R35 GM119812), National Science Foundation (CAREER 1654656), and American Chemical Society Petroleum Research Fund for financial support. L.M.S. is grateful for an NSF Graduate Research Fellowship.Publication History
Received: 06 October 2017
Accepted after revision: 13 November 2017
Publication Date:
12 February 2018 (online)
Abstract
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
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