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State-of-the-art strategies for Lewis acid-catalyzed strain-release cycloadditions of bicyclo[1.1.0]butanes (BCBs)
Organic Chemistry Frontiers ( IF 4.6 ) Pub Date : 2024-10-21 , DOI: 10.1039/d4qo01741b
Xiang Liu, Jiawei He, Keyu Lin, Xingyue Wang, Hua Cao

Due to their low activation energy barriers, small strained carbocyclic systems have always been fascinating building blocks in organic chemistry. Among them, BCBs, as the smallest bicyclic carbocycles, exhibit a molecular structure, bond angles, and orbital hybridization significantly different from those of strain-free hydrocarbons, resulting in unique reactivity. In recent years, Lewis acid-catalyzed strain-release cycloaddition reactions have made BCBs powerful synthetic tools, utilized in various laboratories to expand into other ring systems. This review primarily focuses on the latest developments in Lewis acid-catalyzed strain-release cycloaddition reactions of BCBs, highlighting the applications and limitations of this catalytic system in different types of cycloaddition reactions, providing professionals and non-professionals in the field with valuable insights and new inspiration.

中文翻译:


Lewis 酸催化的双环 [1.1.0] 丁烷 (BCB) 菌株释放环加成反应的最新策略



由于其低活化能势垒,小应变碳环系统一直是有机化学中令人着迷的组成部分。其中,BCBs 作为最小的双环碳环,表现出与无应变碳氢化合物明显不同的分子结构、键角和轨道杂交,从而产生独特的反应性。近年来,Lewis 酸催化的菌株释放环加成反应使 BCB 成为强大的合成工具,在各种实验室中用于扩展到其他环系统。本文主要综述了 Lewis 酸催化的 BCBs 菌株释放环加成反应的最新进展,重点介绍了该催化体系在不同类型的环加成反应中的应用和局限性,为该领域的专业人士和非专业人士提供了有价值的见解和新的启发。
更新日期:2024-10-21
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