Practical, efficient, and broadly applicable synthesis of readily differentiable vicinal diboronate compounds by catalytic three-component reactions

- A practical, cost-effective, efficient, broadly applicable and highly site-selective catalytic method is reported.
- Products are easily differentiable vicinal diboronate compounds that are otherwise difficult to prepare.
- Products may contain tertiary or quaternary boron-substituted carbon stereogenic centers.
- Products contain a terminal alkene that is readily functionalizable.
- Catalytic enantioselective variants are reported.

A practical, efficient and broadly applicable catalytic method for synthesis of easily differentiable vicinal diboronate compounds is presented. Reactions are promoted by a combination of PCy3 or PPh3, CuCl and LiOt-Bu and may be performed with readily accessible alkenyl boronate substrates. Through the use of an alkenyl-B(pin) (pin = pinacolato) or alkenyl-B(dan) (dan = naphthalene-1,8-diaminato) starting material and commercially available (pin)B-B(dan) or B2(pin)2 as the reagent, a range of vicinal diboronates, including those that contain a B-substituted quaternary carbon center, may be prepared in up to 91% yield and with >98% site selectivity. High enantioselectivities can be obtained (up to 96:4 er) through the use of commercially available chiral bis-phosphine ligands for reactions that afford mixed diboronate products.

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