亲核细胞
催化作用
化学
组合化学
反应性(心理学)
三键
分子
有机合成
偶联反应
计算化学
氢键
立体化学
基质(水族馆)
双键
有机化学
医学
海洋学
替代医学
病理
地质学
作者
Megan H. Shaw,Valerie W. Shurtleff,Jack A. Terrett,James D. Cuthbertson,David W. C. MacMillan
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2016-06-10
卷期号:352 (6291): 1304-1308
被引量:467
标识
DOI:10.1126/science.aaf6635
摘要
The use of sp(3) C-H bonds--which are ubiquitous in organic molecules--as latent nucleophile equivalents for transition metal-catalyzed cross-coupling reactions has the potential to substantially streamline synthetic efforts in organic chemistry while bypassing substrate activation steps. Through the combination of photoredox-mediated hydrogen atom transfer (HAT) and nickel catalysis, we have developed a highly selective and general C-H arylation protocol that activates a wide array of C-H bonds as native functional handles for cross-coupling. This mild approach takes advantage of a tunable HAT catalyst that exhibits predictable reactivity patterns based on enthalpic and bond polarity considerations to selectively functionalize α-amino and α-oxy sp(3) C-H bonds in both cyclic and acyclic systems.
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