Multicomponent reactions create diverse α-acyl-β-amino amides from aldehydes and amines, indicating efficiency in synthesis.
Herein, we describe a novel multicomponent synthesis of α-acyl-β-amino amides with structural diversity and brevity from aldehydes, amines, and β-acyloxy alkenyl amides (AAAs). In this multicomponent protocol involving fragmentation and reassembly processes, AAAs act as the key building blocks for the construction of the β-amino amides simply via acid promotion, providing a step- and atom-economical approach to access these useful products with excellent diastereoselectivity.
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Tong et al. (2026) studied this question.
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