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For: Parmeggiani F, Brenna E, Colombo D, Gatti FG, Tentori F, Tessaro D. "A Study in Yellow": Investigations in the Stereoselectivity of Ene-Reductases. Chembiochem 2021. [PMID: 34586700 DOI: 10.1002/cbic.202100445] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Long Z, Li K, Xue Y, Sun Y, Li J, Su Z, Sun J, Liu Q, Liu H, Wei T. Purification and biochemical characterization of a novel ene- reductase from Kazachstania exigua HSC6 for dihydro-β-ionone from β-ionone. Biotechnol Lett 2023. [PMID: 36738355 DOI: 10.1007/s10529-023-03355-1] [Reference Citation Analysis]
2 Sun L, Liu Y, Song H, Hao J, Lin L. Engineering of an ene-reductase for producing the key intermediate of antiepileptic drug Brivaracetam. Appl Microbiol Biotechnol 2023. [PMID: 36710288 DOI: 10.1007/s00253-023-12389-4] [Reference Citation Analysis]
3 Knaus T, Corrado ML, Mutti FG. One-Pot Biocatalytic Synthesis of Primary, Secondary, and Tertiary Amines with Two Stereocenters from α,β-Unsaturated Ketones Using Alkyl-Ammonium Formate. ACS Catal 2022;12:14459-75. [PMID: 36504913 DOI: 10.1021/acscatal.2c03052] [Reference Citation Analysis]
4 Li J, Li J, Cui Y, Wang M, Feng J, Yao P, Wu Q, Zhu D. Asymmetric Synthesis of Both Enantiomers of Dimethyl 2-Methylsuccinate by the Ene-Reductase-Catalyzed Reduction at High Substrate Concentration. Catalysts 2022;12:1133. [DOI: 10.3390/catal12101133] [Reference Citation Analysis]
5 Luan P, Li Y, Huang C, Dong L, Ma T, Liu J, Gao J, Liu Y, Jiang Y. Design of De Novo Three-Enzyme Nanoreactors for Stereodivergent Synthesis of α-Substituted Cyclohexanols. ACS Catal . [DOI: 10.1021/acscatal.2c02136] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Venturi S, Trajkovic M, Colombo D, Brenna E, Fraaije MW, Gatti FG, Macchi P, Zamboni E. Chemoenzymatic Synthesis of the Most Pleasant Stereoisomer of Jessemal. J Org Chem 2022. [PMID: 35442680 DOI: 10.1021/acs.joc.2c00427] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Serra S, Marzorati S, Valentino M. Two Biotechnological Approaches to the Preparative Synthesis of Natural Dihydrocoumarin. Catalysts 2022;12:28. [DOI: 10.3390/catal12010028] [Reference Citation Analysis]