Bietti Massimo
Dipartimento di Scienze e Tecnologie Chimiche, Università "Tor Vergata", Via della Ricerca Scientifica, 1, I-00133, Rome, Italy.
Angew Chem Int Ed Engl. 2018 Dec 17;57(51):16618-16637. doi: 10.1002/anie.201804929. Epub 2018 Nov 8.
Selective functionalization of unactivated aliphatic C-H bonds represents an important goal of modern synthetic chemistry. Differentiating between such bonds in organic molecules with high levels of selectivity remains a crucial issue, and a profound understanding of even the subtlest reactivity trends is needed. Among the methods that have been developed, those based on hydrogen atom transfer (HAT) have attracted considerable interest. Within this framework, medium effects have proved effective in altering the reactivity and site selectivity in synthetically useful C-H functionalization procedures. In this Review, the mechanistic features behind the available strategies are discussed. It is shown that hydrogen bonding and acid-base interactions can promote C-H bond activation or deactivation toward HAT reagents, thereby providing fine-control over the site selectivity and product chemoselectivity as well as useful guidelines for future development and applications.
未活化脂肪族C-H键的选择性官能团化是现代合成化学的一个重要目标。在有机分子中以高选择性区分此类键仍然是一个关键问题,甚至需要对最细微的反应趋势有深刻的理解。在已开发的方法中,基于氢原子转移(HAT)的方法引起了相当大的关注。在此框架内,介质效应已被证明在合成有用的C-H官能团化过程中能有效改变反应性和位点选择性。在本综述中,讨论了现有策略背后的机理特征。结果表明,氢键和酸碱相互作用可以促进C-H键对HAT试剂的活化或失活,从而提供对位点选择性和产物化学选择性的精细控制,以及对未来开发和应用的有用指导。