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Metal-free trans-hydroboration without a B-H bond: reactions of propargyl amines with Lewis acidic boranes.

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The first alkyne trans-hydroboration reaction without a B-H bond was described. This was achieved by reactions of propargyl amines with Lewis acidic boranes under mild conditions. The mechanism involved borane-mediated… Click to show full abstract

The first alkyne trans-hydroboration reaction without a B-H bond was described. This was achieved by reactions of propargyl amines with Lewis acidic boranes under mild conditions. The mechanism involved borane-mediated alkyne activation and intramolecular hydride transfer, thus realizing a unique hydroboration in the absence of a B-H bond.

Keywords: reactions propargyl; without bond; propargyl amines; trans hydroboration; amines lewis; bond

Journal Title: Chemical communications
Year Published: 2022

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