区域选择性
反应性(心理学)
化学
有机合成
脱羧
组合化学
转化式学习
生化工程
有机化学
纳米技术
计算机科学
有机分子
功能群
出处
期刊:ACS omega
[American Chemical Society]
日期:2026-02-12
卷期号:11 (7): 11001-11048
标识
DOI:10.1021/acsomega.5c09198
摘要
Carboxylic acids serve as versatile precursors in modern synthesis, leveraging decarboxylative strategies to bypass traditional reactivity patterns and facilitate the generation of high-energy intermediates. This transformative approach enables streamlined molecular assembly and enhances structural diversification through the regioselective removal of CO2. This review provides a high-level, comprehensive synthesis of recent breakthroughs in decarboxylation, transitioning from traditional thermal methods to cutting-edge reactivity paradigms. We critically evaluate diverse catalytic systems, including transition metal-catalyzed processes (Fe, Ni, Cu, Zn, Ag, Ti, Ce, Ru, and In), Pd-catalyzed cross-couplings, and the burgeoning fields of organocatalysis, photoredox catalysis, and electrosynthetic mediation. Beyond a mere survey of reaction conditions, this work dissects mechanistic intricacies and addresses the inherent challenges of regioselectivity and functional group tolerance. By highlighting the assembly of complex molecular architectures from these ubiquitous precursors, this review establishes a conceptual framework intended to catalyze the next generation of innovations in decarboxylative chemistry and to inspire the discovery of novel reactivity manifolds.
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