Interlocking Pseudorotaxanes through Borane- and Boronic Ester-Mediated Carbon–Carbon Bond Formation
Journal
Organic Letters
Journal Volume
27
Journal Issue
18
Start Page
4772
End Page
4776
ISSN
1523-7060
1523-7052
Date Issued
2025-04-30
Author(s)
Abstract
Employing 9-BBN and pinacol boronic ester as surrogate stoppers, pseudorotaxanes presenting terminal alkenes can be transformed into organoborane or organoboronate rotaxanes, respectively. Various boron-based reactions can then be used to replace these temporary stoppers with bulky derivatives of aromatic bromides, α-bromo ketones, or 1-bromo-1-alkynes, facilitating the selective formation of sp3-sp2, sp3-sp3, and sp3-sp carbon-carbon single bonds, respectively.
SDGs
Publisher
American Chemical Society (ACS)
Type
journal article
