Dang Nhu, San Martin Jovan, Shaikh Melad, Yan Yong
Department of Chemistry and Biochemistry, San Diego State University, San Diego, California 92182, United States.
J Am Chem Soc. 2025 May 21;147(20):17273-17280. doi: 10.1021/jacs.5c03588. Epub 2025 May 8.
Directly introducing aliphatic or aromatic amines into C(sp)-H bonds remains a significant challenge in organic synthesis. One major difficulty is that C(sp)-H activation is an oxidative process, whereas amines are generally more prone to oxidation than C-H bonds, making them difficult to use directly. Typically, protected amines are employed and then deprotected to realize amination, but this strategy limits the synthesis of tertiary amines, as protected secondary amines are often inactive in such reactions. Here, we present a mild photocatalytic method that overcomes these limitations by utilizing Ni-doped perovskite CsPbBr nanocrystals (NCs) for benzylic C-H amination directly using unprotected aliphatic or aromatic amines. Perovskite enables highly selective C-H activation, while doped Ni(II) readily captures benzylic radicals via oxidative addition. XPS studies successfully validate such an oxidative addition step with a Ni(II)/Ni(III) configuration. Our methodology forges aromatic and aliphatic, cyclic and acyclic, and secondary and tertiary amines and provides a powerful tool for the late-stage functionalization of bioactive compounds and drug derivatives.
在有机合成中,将脂肪族或芳香族胺直接引入C(sp) - H键仍然是一项重大挑战。一个主要困难在于,C(sp) - H活化是一个氧化过程,而胺类通常比C - H键更容易被氧化,这使得它们难以直接使用。通常,会使用受保护的胺类,然后进行脱保护以实现胺化,但这种策略限制了叔胺的合成,因为受保护的仲胺在此类反应中往往没有活性。在此,我们提出了一种温和的光催化方法,该方法通过利用镍掺杂的钙钛矿CsPbBr纳米晶体(NCs),直接使用未受保护的脂肪族或芳香族胺进行苄基C - H胺化,从而克服了这些限制。钙钛矿能够实现高度选择性的C - H活化,而掺杂的Ni(II)通过氧化加成容易捕获苄基自由基。XPS研究成功验证了这种具有Ni(II)/Ni(III)构型的氧化加成步骤。我们的方法可构建芳香族和脂肪族、环状和非环状以及仲胺和叔胺,并为生物活性化合物和药物衍生物的后期功能化提供了一个强大的工具。