双环[1.1.0]丁烷和[1.1.1]丙烷的应变释放转化

Qian-Qian Hu , Jie Chen , Yang Yang , Hui Yang , Ling Zhou
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引用次数: 0

摘要

双环[1.1.0]丁烷(BCBs)和[1.1.1]丙烷(三环[1.1.1.01,3]戊烷,TCPs)是结构独特的化合物,具有不同的化学特性。应变释放驱动反应已成为一种原子和步骤经济的有机合成策略。利用这种策略,可以高效合成各种功能环分子,包括各种环丁烷分子、双环[2.1.1]己烷、双环[1.1.1]戊烷等。更具体地说,这些应变释放驱动的反应包括亲核加成、自由基加成、亲电或过渡金属催化等方面。本综述将讨论双环[1.1.0]丁烷和[1.1.1]丙烷应变释放转化的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes

Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes

Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties. Strain-release driven reactions have emerged as an atom- and step-economic strategy for the organic synthesis. Using this strategy, a variety of functional ring molecules have been efficiently synthesized, including various cyclobutane molecules, bicyclo[2.1.1]hexanes, bicyclo[1.1.1]pentanes, and others. More specifically, these strain release-driven reactions include aspects of nucleophilic addition, radical addition, electrophilic or transition metal catalysis. This review will discuss the recent developments in the strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes.

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来源期刊
Tetrahedron chem
Tetrahedron chem Organic Chemistry
CiteScore
3.60
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27 days
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