This paper summarizes recent advancements in asymmetric reactions of isocyanides, highlighting their potential in diverse chiral scaffold synthesis.
Beyond the conventional carbon-centered chirality, catalytic asymmetric transformations of isocyanides have recently emerged as a powerful strategy for the efficient synthesis of structurally diverse scaffolds featuring axial, planar, helical, and inherent chirality. Herein, we summarize the exciting achievements in this rapidly evolving field. These elegant examples have been organized and presented based on the reaction type as well as the resulting chirality form. Additionally, we provide a perspective on the current limitations and future opportunities, aiming to inspire further advances in this area.
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Jia‐Yu Liao (2025) studied this question.
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