As a member of the suzuki coupling reaction, the reactions 4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane participates in are mostly mild and controlled, and it can be used in the synthesis of many natural products and materials. Compared with the same type of bis(pinacolato)diboron, it has higher efficiency, lower toxicity and non-toxic by-products. At the same time, 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane is liquid, which is convenient for reaction feeding and easy for post-reaction processing.
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