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脱羧偶联反应:C-C 键形成的现代策略。

Decarboxylative coupling reactions: a modern strategy for C-C-bond formation.

机构信息

FB Chemie-Organische Chemie, TU Kaiserslautern, Erwin-Schrödinger-Strasse, Geb. 54, 67663 Kaiserslautern, Germany.

出版信息

Chem Soc Rev. 2011 Oct;40(10):5030-48. doi: 10.1039/c1cs15093f. Epub 2011 Jul 27.

Abstract

This critical review examines transition metal-catalyzed decarboxylative couplings that have emerged within recent years as a powerful strategy to form carbon-carbon or carbon-heteroatom bonds starting from carboxylic acids. In these reactions, C-C bonds to carboxylate groups are cleaved, and in their place, new carbon-carbon bonds are formed. Decarboxylative cross-couplings constitute advantageous alternatives to traditional cross-coupling or addition reactions involving preformed organometallic reagents. Decarboxylative reaction variants are also known for Heck reactions, direct arylation processes, and carbon-heteroatom bond forming reactions.

摘要

这篇评论性文章考察了近年来新兴的过渡金属催化脱羧偶联反应,该反应是一种从羧酸出发构建碳-碳或碳-杂原子键的有力策略。在这些反应中,羧酸根的 C-C 键被切断,同时形成新的碳-碳键。与涉及预先形成的有机金属试剂的传统交叉偶联或加成反应相比,脱羧交叉偶联具有优势。脱羧反应变体还包括 Heck 反应、直接芳基化过程和碳-杂原子键形成反应。

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