Hydroboration without a B–H bond: reactions of the borinium cation [(iPr2N)2B]+ with alkyne, nitrile, ketone and diazomethane†
Abstract
The borinium cation [(iPr2N)2B]+ (1+) is shown to react with PhCCH, PhCN, Ph2CO, and Ph2CN2 to effect a net hydroboration, affording borenium complexes of the form [(iPr2N)B(iPrNCMe2)(L)][B(C6F5)4] (L = CHCHPh 2, NCHPh 3, OCHPh24, NHNCPh25). The nature and reaction of 1+ with PhCCH was probed computationally and the reduction of these unsaturates is shown to occur via hydride transfer from an isopropyl group to the alkyne, thus effecting hydroboration without a B–H bond.
- This article is part of the themed collection: Editor’s Choice: Main group reagents and catalysts in organic reactions