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DOI: 10.1055/a-2680-9502
Chiral-Pyridoxal-Catalyzed Biomimetic Aldol Reaction of Glycinate with Aldehydes
Autoren
Asymmetric Biomimetic Aldol Reaction of Glycinate Enables Highly Efficient Synthesis of Chiral β-Hydroxy-α-Amino Acid Derivatives.
Nat. Catal. 2025;
8: 668-677
DOI: 10.1038/s41929-025-01364-z

Significance
Zhao, Xiao, and co-workers report a broadly applicable strategy using a chiral pyridoxal catalyst to promote highly efficient and stereoselective biomimetic aldol reactions across a wide substrate scope. Using a high-throughput asymmetric synthesis platform has enabled the generation of over 1,700 diverse β-hydroxy-α-amino acid derivatives, offering a valuable chiral library for drug discovery.
Comment
This work represents an advancement in biomimetic catalysis through the development of chiral pyridoxal catalysts for the aldol reaction between glycinate and aldehydes. Moreover, the success of these pyridoxal-based catalysts greatly expands the chemical repertoire of vitamin B6 mimetic systems, providing new insights into the catalytic mechanisms of PLP (pyridoxal 5′-phosphate)-dependent enzymes.
Publikationsverlauf
Artikel online veröffentlicht:
23. September 2025
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