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钯催化游离羧酸的 C(sp )-H 功能化的出现。

The Emergence of Palladium-Catalyzed C(sp )-H Functionalization of Free Carboxylic Acids.

机构信息

Indian Institute of Science Education and Research Kolkata Nadia, West Bengal, India.

出版信息

Chem Asian J. 2021 Mar 1;16(5):397-408. doi: 10.1002/asia.202001440. Epub 2021 Feb 2.

Abstract

Palladium-catalyzed directing group assisted C-H bond activation has emerged as a powerful tool in synthetic organic chemistry. However, only recently, among various directing groups, widely available carboxylate moiety is recognized as a versatile candidate for the regioselective transformations. Notably, palladium-catalyzed carboxylate directed C(sp )-H bond activation and diverse functionalization is highly challenging and has gained huge attention for its versatile applications. Mono- and bidentate ligands have proven to be useful for accelerating the C(sp )-H bond activation step, which helps to control reactivity and selectivity (including enantioselectivity). In this Minireview, we discuss the recent progress made in palladium-catalyzed C(sp )-H bond functionalization reactions for the construction of C-C and C-Heteroatom bonds with the direction of free carboxylic acid.

摘要

钯催化导向基团辅助 C-H 键活化已成为合成有机化学中一种强大的工具。然而,直到最近,在各种导向基团中,广泛存在的羧酸盐部分才被认为是区域选择性转化的多功能候选物。值得注意的是,钯催化的羧酸盐导向 C(sp )-H 键活化和多样化的功能化具有很大的挑战性,并因其广泛的应用而受到极大关注。单齿和双齿配体已被证明可用于加速 C(sp )-H 键活化步骤,这有助于控制反应性和选择性(包括对映选择性)。在这篇综述中,我们讨论了最近在钯催化的 C(sp )-H 键功能化反应方面取得的进展,这些反应是在游离羧酸的导向下构建 C-C 和 C-杂原子键。

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