Copper(I)-Thiazol-2-ylidenes: Highly Reactive N-Heterocyclic Carbenes for the Hydroboration of Terminal and Internal Alkynes. Ligand Development, Synthetic Utility, and Mechanistic Studies

In the last 15 years, copper-catalyzed borylative transformations utilizing boryl-copper have been established as a powerful activation mode in organic synthesis and catalysis, enabling direct transformations of various pi-systems. Although many of these transformations use NHC (N-heterocyclic carbene) ligands, these studies have been almost exclusively limited to the derivatives of imidazol-2-ylidenes. However, the molecular properties of N-aryl-imidazol-2-ylidenes, such as IPr (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene), are limited by (1) the high degree of heteroatom stabilization and (2) symmetrical substitution of the nitrogen atoms. Herein, we report a study on Cu(I)-thiazol-2-ylidenes, thiazole analogues of imidazol-2-ylidenes, which (1) feature a distinct half-umbrella shape of the coordinating ligand and (2) exhibit lower heteroatom stabilization of the ancillary ligand through reduced pi-donation from sulfur. We present the development of a family of stable Cu(I)-thiazol-2-ylidenes, where the combined sterics of thiazol-2-ylidenes lead to monomers [Cu(NHC)X] or bridged-halo dimers [Cu(NHC) (mu-X)]2, their crystallographic characteristics, and application to the hydroboration of alkynes to afford trisubstituted vinylboronates by ,g- hydroboration of internal alkynes or terminal vinylboronates by ,g-hydroboration of terminal alkynes. Application to the late-stage modification and detailed mechanistic studies on the catalyst structure and activation are presented. Most crucially, Cu(I)-thiazol-2-ylidenes show a much higher ,g-selectivity in the hydroboration of alkynes than that of classical imidazol-2-ylidenes, affording vinylborons in excellent yields at ambient conditions. The unique "half-umbrella" shape of thiazol-2-ylidenes reverses the alpha/,g regioselectivity observed with imidazol-2-ylidenes in the hydroboration of terminal alkynes. Kinetic studies demonstrate that Cu(I)- thiazol-2-ylidenes supersede imidazol-2-ylidenes. Considering the significant utility of borylative transformations of pi-systems, we anticipate that Cu(I)-thiazol-2-ylidenes will advance the synthetic transformations of boryl-copper in organic synthesis and catalysis.