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Updated: May 16, 2025

Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
Interlocking Pseudorotaxanes through Borane- and Boronic Ester-Mediated Carbon-Carbon Bond Formation
Jia-Jyun Jian1, Min-Xuan Zhang1, Yi-Hung Liu1
1Department of Chemistry, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 106, Taiwan.
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.
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