The first copper-catalyzed enantioselective allylboration of alkynes is reported. The method employs a multitasking chiral NHC-Cu catalyst and provides access to densely functionalized molecules from simple starting materials with excellent levels of chemo-, regio-, and enantioselectivity. These multifunctional products display highly versatile reactivity as shown by the synthesis of a variety of non-racemic molecular scaffolds. DFT calculations were conducted to gain insight into the high selectivity levels of this catalytic process.
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Rivera‐Chao et al. (2019) studied this question.
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