Catalyst-Free Propargylboration of Ketones with Allenyl-Bpins: Highly Stereoselective Synthesis of tert-Homopropargyl Alcohols Bearing Vicinal Stereocenters.

Abstract

A practical and efficient propargylboration of ketones is presented using general allenylboronic acid pinacol esters (allenyl-Bpins) without a catalyst. This reaction is triggered by in-situ activation of stable allenyl-Bpins through the sequential addition of 1.25 equiv. of n BuLi and the prerequisite 2.0 equiv. of TFAA. Under the optimized reaction conditions, the versatile trisubstituted allenyl-Bpins react with various ketones smoothly to afford a wide range of tert-homopropargyl alcohols bearing vicinal stereocenters in high yields with good to excellent diastereoselectivities. Furthermore, propargylboration of ketones with chiral trisubstituted allenyl-Bpins allows for the asymmetric synthesis of chiral tert-homopropargyl alcohols with a full chirality transfer.