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(iPrN![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) CMe2)(L)][B(C6F5)4] (L = CH
CMe2)(L)][B(C6F5)4] (L = CH![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) CHPh 2, N
CHPh 2, N![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) CHPh 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.
CHPh 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
 
                




 Please wait while we load your content...
                                            Please wait while we load your content...
                                        