Godula Kamil, Sames Dalibor
Department of Chemistry, Columbia University, 3000 Broadway, New York, NY 10027, USA.
Science. 2006 Apr 7;312(5770):67-72. doi: 10.1126/science.1114731.
Direct and selective replacement of carbon-hydrogen bonds with new bonds (such as C-C, C-O, and C-N) represents an important and long-standing goal in chemistry. These transformations have broad potential in synthesis because C-H bonds are ubiquitous in organic substances. At the same time, achieving selectivity among many different C-H bonds remains a challenge. Here, we focus on the functionalization of C-H bonds in complex organic substrates catalyzed by transition metal catalysts. We outline the key concepts and approaches aimed at achieving selectivity in complex settings and discuss the impact these reactions have on synthetic planning and strategy in organic synthesis.
用新的化学键(如C-C、C-O和C-N)直接且选择性地取代碳-氢键是化学领域一个重要且长期存在的目标。这些转化在合成中具有广泛的潜力,因为碳-氢键在有机物质中普遍存在。同时,在众多不同的碳-氢键中实现选择性仍然是一项挑战。在此,我们聚焦于过渡金属催化剂催化的复杂有机底物中碳-氢键的官能团化。我们概述了旨在在复杂环境中实现选择性的关键概念和方法,并讨论了这些反应对有机合成中的合成规划和策略的影响。