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A new approach to chiral α-amino acid synthesis - photo-driven nitrogen heterocyclic carbene catalyzed highly enantioselective radical α-amino esterification

Researchers at Tsinghua University developed a novel method for synthesizing chiral alpha-amino acids using a photo-driven nitrogen heterocyclic carbene catalyst. The reaction achieves good to excellent enantioselectivity and substrate versatility, enabling the rapid preparation of structurally diverse chiral alpha-amino acid derivatives.

SourceChinese Chemical Society·JournalCCS Chemistry·TypeExperimental study·DateJan 30, 2026

Salts as building blocks for organocatalysis

Researchers from Ruhr-University Bochum developed a novel approach to create salts that catalyze specific reactions. The cation and anion components of the salt play crucial roles in ensuring the correct handedness of the resultant molecule.

SourceRuhr-University Bochum·JournalJournal of the American Chemical Society·TypeExperimental study·DateMar 6, 2025

Robots and A.I. team up to discover highly selective catalysts

Researchers developed a machine learning model using advanced 2D chemical descriptors to predict highly selective asymmetric catalysts without quantum chemical computations. The model demonstrated high accuracy in predicting catalyst structures and selectivity, outperforming existing methods.

SourceHokkaido University·JournalAngewandte Chemie International Edition·TypeExperimental study·DateFeb 2, 2023

New methodology for the synthesis of benzazepines, a highly interesting bioactive molecule

Researchers at CiQUS developed a new methodology for synthesizing chiral benzazepines, a highly interesting bioactive molecule. The method uses a palladium metal and a newly designed chiral ligand to activate specific C-H bonds, enabling the efficient production of these compounds.

SourceCenter for Research in Biological Chemistry and Molecular Materials (CiQUS)·JournalJournal of the American Chemical Society·TypeExperimental study·DateDec 15, 2022