Issue 91, 2023

Skeletal rearrangement of a boron-containing annulenic molecule into a macrocycle bridged by an electronically stabilized boron cation

Abstract

An annulenic molecule containing a three-coordinate chloroborane moiety, which exhibits a borane-olefin proximity effect, undergoes a skeletal rearrangement upon chloride abstraction, to generate a three-dimensional macrocyclic molecule featuring a borocenium (η5-cyclopentadienyl–B+–R) structure.

Graphical abstract: Skeletal rearrangement of a boron-containing annulenic molecule into a macrocycle bridged by an electronically stabilized boron cation

Supplementary files

Article information

Article type
Communication
Submitted
28 Sep 2023
Accepted
23 Oct 2023
First published
24 Oct 2023

Chem. Commun., 2023,59, 13635-13638

Author version available

Skeletal rearrangement of a boron-containing annulenic molecule into a macrocycle bridged by an electronically stabilized boron cation

Y. Murata, C. Özen, S. Maeda, T. Fukushima and Y. Shoji, Chem. Commun., 2023, 59, 13635 DOI: 10.1039/D3CC04830F

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