第1章。碳氢键功能化中的非共价相互作用

K. Mahmudov, A. Gurbanov, M. F. C. G. Silva, A. Pombeiro
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引用次数: 2

摘要

在过去的几十年里,将C - h键直接功能化/激活为C - E (E = C, N, O, S,金属等)键已成为现代合成化学中最有价值和最直接的方法之一。同时,由于分子内各种碳氢键的反应性存在细微差异,控制碳氢键的选择性仍然是碳氢键催化功能化/活化的核心挑战。在本章中,我们讨论了非共价相互作用在烷烃、烯烃、炔烃、芳烃、杂环化合物、醛类和酮类化合物的C-H键功能化中的关键作用。这些弱力在中间体的形成/稳定以及控制反应的选择性和结果方面是强有力的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CHAPTER 1. Noncovalent Interactions in C–H Bond Functionalization
Over the past few decades, direct functionalization/activation of the C–H bond to C–E (E = C, N, O, S, metal, etc.) bonds has become one of the most valuable and straightforward protocols in modern synthetic chemistry. In parallel, controlling the selectivity remains a central challenge in the catalytic functionalization/activation of C–H bond(s) owing to the subtle differences in the reactivity of the various C–H bonds within the molecule. In this chapter, we discuss the crucial role of noncovalent interactions in C–H bond functionalization in alkanes, alkenes, alkynes, aromatics, heterocyclics, aldehydes and ketones. These weak forces can be powerful tools in the formation/stabilization of intermediates and in controlling the selectivity and outcome of a reaction.
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