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Cited by in F6Publishing
For: Li M, Cui Y, Xu Z, Chen X, Feng J, Wang M, Yao P, Wu Q, Zhu D. Asymmetric Synthesis of N ‐Substituted γ‐Amino Esters and γ‐Lactams Containing α,γ‐Stereogenic Centers via a Stereoselective Enzymatic Cascade. Adv Synth Catal 2022;364:372-9. [DOI: 10.1002/adsc.202100953] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Yang L, Li J, Xu Z, Yao P, Wu Q, Zhu D, Ma Y. Asymmetric Synthesis of Fused-Ring Tetrahydroisoquinolines and Tetrahydro-β-carbolines from 2-Arylethylamines via a Chemoenzymatic Approach. Org Lett 2022. [PMID: 36066397 DOI: 10.1021/acs.orglett.2c02466] [Reference Citation Analysis]
3 Zhan Z, Xu Z, Yu S, Feng J, Liu F, Yao P, Wu Q, Zhu D. Stereocomplementary Synthesis of a Key Intermediate for Tofacitinib via Enzymatic Dynamic Kinetic Resolution‐Reductive Amination. Adv Synth Catal. [DOI: 10.1002/adsc.202200361] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Carballares D, Rocha-Martin J, Fernandez-Lafuente R. Chemical amination of immobilized enzymes for enzyme coimmobilization: Reuse of the most stable immobilized and modified enzyme. Int J Biol Macromol 2022;208:688-97. [PMID: 35358572 DOI: 10.1016/j.ijbiomac.2022.03.151] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
5 Kumar Roy T, Sreedharan R, Ghosh P, Gandhi T, Maiti D. Ene-Reductase: A Multifaceted Biocatalyst in Organic Synthesis. Chemistry 2022;28:e202103949. [PMID: 35133702 DOI: 10.1002/chem.202103949] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]