Grover Jagrit, Sebastian Amal Tom, Maiti Siddhartha, Bissember Alex C, Maiti Debabrata
Department of Chemistry, IIT Bombay, Powai, Mumbai-400076, India.
VIT Bhopal University School of Biosciences Engineering & Technology, India.
Chem Soc Rev. 2025 Feb 17;54(4):2006-2053. doi: 10.1039/d0cs00488j.
In organic synthesis, C(sp)-H functionalization is a revolutionary method that allows direct alteration of unactivated C-H bonds. It can obviate the need for pre-functionalization and provides access to streamlined and atom economical routes for the synthesis of complex molecules starting from simple starting materials. Many strategies have evolved, such as photoredox catalysis, organocatalysis, non-directed C-H activation, transiently directed C-H activation, and native functionality directed C-H activation. Together these advances have reinforced the importance of C(sp)-H functionalization in synthetic chemistry. C(sp)-H functionalization has direct applications in pharmacology, agrochemicals, and materials science, demonstrating its ability to transform synthetic approaches by creating new retrosynthetic disconnections and boost the efficiency of chemical processes. This review aims to provide an overview of current state of C(sp)-H functionalization, focusing more on recent breakthroughs and associated mechanistic insights.
在有机合成中,C(sp) - H官能团化是一种革命性的方法,它能够直接改变未活化的C - H键。它无需预官能团化,为从简单起始原料合成复杂分子提供了简洁且原子经济的路线。许多策略已经发展起来,例如光氧化还原催化、有机催化、非导向C - H活化、瞬态导向C - H活化以及天然官能团导向C - H活化。这些进展共同强化了C(sp) - H官能团化在合成化学中的重要性。C(sp) - H官能团化在药理学、农用化学品和材料科学中有直接应用,通过创造新的逆合成切断方式展现了其改变合成方法的能力,并提高了化学过程的效率。本综述旨在概述C(sp) - H官能团化的当前状态,更多地关注近期的突破及相关的机理见解。