Tri-insertion with dearomatization of terminal arylalkynes using a carborane based frustrated Lewis pair template.

Abstract

Intramolecular vicinal Frustrated Lewis Pairs (FLPs) have played a significant role in the activation of small molecules, and their stabilities and reactivities are found to strongly depend on the nature of the bridging units. This work reports a new carborane based FLP, 1-PPh2-2-BPh2-1,2-C2B10H10 (2), which reacts with an equimolar amount of p-R2NC6H4C Created by potrace 1.16, written by Peter Selinger 2001-2019 ]]> CH (R = Me, Et, Ph) at room temperature to give CC triple bond addition products 1,2-[PPh2C(R2NC6H4) Created by potrace 1.16, written by Peter Selinger 2001-2019 ]]> CHBPh2]-1,2-C2B10H10 (3) in high yields. Compounds 3 react further with two equiv. of p-R2NC6H4CCH (R = Me, Et) at 60–70 °C to give unprecedented stereoselective tri-insertion products, 3,3a,6,6a-tetrahydronaphtho[1,8a-b]borole tricycles (4), in which one of the aryl rings from arylacetylene moieties has been dearomatized with the formation of four stereocenters including one quaternary carbon center. It is noted that the phosphine unit functions as a catalyst during the reactions. After trapping and structural characterization of a key intermediate, a reaction mechanism is proposed, involving sequential alkyne insertion and 1,2-boryl migration.