Issue 36, 2017

Reactivity of the geminal phosphinoborane tBu2PCH2BPh2 towards alkynes, nitriles, and nitrilium triflates

Abstract

The reactivity of the geminal phosphinoborane tBu2PCH2BPh2 towards terminal alkynes, nitriles and nitrilium salts is investigated. Terminal alkynes react via C–H bond splitting (deprotonation) resulting in the formation of phosphonium borates. In contrast, both nitriles and nitrilium salts undergo addition reactions resulting in the formation of five-membered heterocycles. All compounds were characterized by multinuclear NMR spectroscopy, and single-crystal X-ray structure determinations. Insight into the reaction mechanisms was gained by DFT calculations.

Graphical abstract: Reactivity of the geminal phosphinoborane tBu2PCH2BPh2 towards alkynes, nitriles, and nitrilium triflates

Supplementary files

Article information

Article type
Paper
Submitted
14 Jul 2017
Accepted
26 Aug 2017
First published
28 Aug 2017

Dalton Trans., 2017,46, 12284-12292

Reactivity of the geminal phosphinoborane tBu2PCH2BPh2 towards alkynes, nitriles, and nitrilium triflates

E. R. M. Habraken, L. C. Mens, M. Nieger, M. Lutz, A. W. Ehlers and J. C. Slootweg, Dalton Trans., 2017, 46, 12284 DOI: 10.1039/C7DT02570J

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