Issue 14, 2016

Synthesis of 2-(lutidinyl)organoboranes and their reactivities against dihydrogen and pinacol borane

Abstract

Two 2,4,6-tris(trifluoromethyl)phenyl-substituted 2-(lutidinyl)organoboranes (5a and 5b) were prepared. These complexes can function as intramolecular vicinal B/N frustrated Lewis pairs to heterolytically activate dihydrogen. When these complexes were treated with HBpin, two different reaction pathways took place. Whereas the reaction between 5a and HBpin affords a formal ligand-redistribution product, the reaction of 5b with HBpin leads to a dearomative dehydroborylation product.

Graphical abstract: Synthesis of 2-(lutidinyl)organoboranes and their reactivities against dihydrogen and pinacol borane

Supplementary files

Article information

Article type
Paper
Submitted
30 九月 2015
Accepted
15 十月 2015
First published
20 十月 2015

Dalton Trans., 2016,45, 6088-6093

Author version available

Synthesis of 2-(lutidinyl)organoboranes and their reactivities against dihydrogen and pinacol borane

J. Zheng, Y. Lin and H. Wang, Dalton Trans., 2016, 45, 6088 DOI: 10.1039/C5DT03815D

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