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...

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Bibliographic Details
Main Authors: Qian-Qian Hu, Jie Chen, Yang Yang, Hui Yang, Ling Zhou
Format: Article
Language:English
Published: Elsevier 2024-03-01
Series:Tetrahedron Chem
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666951X24000093
Description
Summary: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.
ISSN:2666-951X