{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ni Z"],"funding":["Chinese Medicine Resources","Shenzhen Science and Technology Innovation Program","CAMS Innovation Fund for Medical Sciences (CIFMS)","Guangdong Basic and Applied Basic Research Foundation","Basic and Applied Basic Research Foundation of Guangdong Province","National Natural Science Foundation of China","Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences","Shenzhen Science and Technology Program"],"pagination":["e10455"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12677705"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["12(45)"],"pubmed_abstract":["As an efficient and environmentally benign strategy, enzymatic catalysis has emerged with high reactivity and selectivity for atropisomeric structures. Atropisomeric biaryl amines are of great importance in drug development and asymmetric catalysis. However, substrates with steric hindrance are often poorly accepted by enzymes, as the immense pockets required are not commonly found in wild-type enzymes. In this work, an imine reductase (IRED)-catalyzed dynamic kinetic resolution (DKR) strategy is introduced for the synthesis of atropisomeric biaryl amines, especially those with bulky substitutions on (hetero)aryls, including naphthalene- and quinoline-containing biaryl scaffolds. A broad range of atropisomeric biaryl amines are obtained in up to 99% yield and 99% ee, enabled by the steric "],"journal":["Advanced science (Weinheim, Baden-Wurttemberg, Germany)"],"pubmed_title":["Steric-Adaptive Biocatalysis: Imine Reductase-Mediated Dynamic Kinetic Resolution for Atroposelective Synthesis of Hindered Biaryl Amines."],"pmcid":["PMC12677705"],"funding_grant_id":["2060302","2023B1515020052","2022-RC350-03","22422110","RCYX20200714114736199","22173077","22371302","2023-I2M-2-006"],"pubmed_authors":["Ni Z","Liu Z","Su P","Cheng GJ","Gao Y","Yang LC","Gao G","Zhuang J"],"additional_accession":[]},"is_claimable":false,"name":"Steric-Adaptive Biocatalysis: Imine Reductase-Mediated Dynamic Kinetic Resolution for Atroposelective Synthesis of Hindered Biaryl Amines.","description":"As an efficient and environmentally benign strategy, enzymatic catalysis has emerged with high reactivity and selectivity for atropisomeric structures. Atropisomeric biaryl amines are of great importance in drug development and asymmetric catalysis. However, substrates with steric hindrance are often poorly accepted by enzymes, as the immense pockets required are not commonly found in wild-type enzymes. In this work, an imine reductase (IRED)-catalyzed dynamic kinetic resolution (DKR) strategy is introduced for the synthesis of atropisomeric biaryl amines, especially those with bulky substitutions on (hetero)aryls, including naphthalene- and quinoline-containing biaryl scaffolds. A broad range of atropisomeric biaryl amines are obtained in up to 99% yield and 99% ee, enabled by the steric ","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Dec","modification":"2026-06-05T23:12:24.968Z","creation":"2026-05-23T03:13:49.33Z"},"accession":"S-EPMC12677705","cross_references":{"pubmed":["41013902"],"doi":["10.1002/advs.202510455"]}}