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For: Wu S, Snajdrova R, Moore JC, Baldenius K, Bornscheuer UT. Biokatalyse: Enzymatische Synthese für industrielle Anwendungen. Angew Chem 2021;133:89-123. [DOI: 10.1002/ange.202006648] [Cited by in Crossref: 62] [Cited by in F6Publishing: 62] [Article Influence: 31.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang Y, Zhao Q, Haag R, Wu C. Biocatalytic Synthesis Using Self‐Assembled Polymeric Nano‐ and Microreactors. Angew Chem Int Ed 2022. [DOI: 10.1002/anie.202213974] [Reference Citation Analysis]
2 Jurkaš V, Weissensteiner F, De Santis P, Vrabl S, Sorgenfrei FA, Bierbaumer S, Kara S, Kourist R, Wangikar PP, Winkler CK, Kroutil W. Transmembrane Shuttling of Photosynthetically Produced Electrons to Propel Extracellular Biocatalytic Redox Reactions in a Modular Fashion. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202207971] [Reference Citation Analysis]
3 Rodriguez‐abetxuko A, Reifs A, Sánchez‐dealcázar D, Beloqui A. A Versatile Chemoenzymatic Nanoreactor that Mimics NAD(P)H Oxidase for the In Situ Regeneration of Cofactors. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202206926] [Reference Citation Analysis]
4 Romero E, Johansson MJ, Cartwright J, Grogan G, Hayes MA. Oxalate Oxidase for In Situ H 2 O 2 ‐Generation in Unspecific Peroxygenase‐Catalysed Drug Oxyfunctionalisations**. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202207831] [Reference Citation Analysis]
5 Rosenthal K, Bornscheuer UT, Lütz S. Cascades of Evolved Enzymes for the Synthesis of Complex Molecules. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202208358] [Reference Citation Analysis]
6 Rosenthal K, Bornscheuer UT, Lütz S. Reaktionskaskaden evolvierter Enzyme zur Synthese komplexer Moleküle. Angewandte Chemie. [DOI: 10.1002/ange.202208358] [Reference Citation Analysis]
7 Meyer L, Andersen MB, Kara S. A Deep Eutectic Solvent Thermomorphic Multiphasic System for Biocatalytic Applications. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202203823] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Zhao F, Lauder K, Liu S, Finnigan JD, Charnock SBR, Charnock SJ, Castagnolo D. Chemoenzymatic Cascades for the Enantioselective Synthesis of β-Hydroxysulfides Bearing a Stereocentre at the C-O or C-S Bond by Ketoreductases. Angew Chem Int Ed Engl 2022;61:e202202363. [PMID: 35576553 DOI: 10.1002/anie.202202363] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Xia H, Song J, Li C, Xue F. Recent developments in promiscuous enzymatic reactions for carbon-nitrogen bond formation. Bioorg Chem 2022;127:106014. [PMID: 35841668 DOI: 10.1016/j.bioorg.2022.106014] [Reference Citation Analysis]
10 Li R, Kong W, An Z. Enzyme Catalysis for Reversible Deactivation Radical Polymerization. Angew Chem Int Ed Engl 2022;61:e202202033. [PMID: 35212121 DOI: 10.1002/anie.202202033] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
11 Meyer L, Andersen MB, Kara S. Ein thermomorphes stark eutektisches Lösungsmittelmehrphasensystem für biokatalytische Anwendungen. Angewandte Chemie. [DOI: 10.1002/ange.202203823] [Reference Citation Analysis]
12 Fang J, Turner LE, Chang MCY. Biocatalytic Asymmetric Construction of Secondary and Tertiary Fluorides from β-Fluoro-α-Ketoacids. Angew Chem Int Ed Engl 2022;61:e202201602. [PMID: 35165991 DOI: 10.1002/anie.202201602] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Fessner ND, Badenhorst CPS, Bornscheuer UT. Enzyme Kits to Facilitate the Integration of Biocatalysis into Organic Chemistry – First Aid for Synthetic Chemists. ChemCatChem. [DOI: 10.1002/cctc.202200156] [Reference Citation Analysis]
14 Labib M, Grabowski L, Brüsseler C, Kallscheuer N, Wachtendonk L, Fuchs T, Jupke A, Wiechert W, Marienhagen J, Rother D, Noack S. Toward the Sustainable Production of the Active Pharmaceutical Ingredient Metaraminol. ACS Sustainable Chem Eng 2022;10:5117-28. [DOI: 10.1021/acssuschemeng.1c08275] [Reference Citation Analysis]
15 Wied P, Carraro F, Bolivar JM, Doonan CJ, Falcaro P, Nidetzky B. Combining a Genetically Engineered Oxidase with Hydrogen-Bonded Organic Frameworks (HOFs) for Highly Efficient Biocomposites. Angew Chem Int Ed Engl 2022;61:e202117345. [PMID: 35038217 DOI: 10.1002/anie.202117345] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
16 Fang J, Turner LE, Chang MCY. Biocatalytic Asymmetric Construction of Secondary and Tertiary Fluorides from β‐Fluoro‐α‐Ketoacids**. Angewandte Chemie. [DOI: 10.1002/ange.202201602] [Reference Citation Analysis]
17 Greifenstein R, Ballweg T, Hashem T, Gottwald E, Achauer D, Kirschhöfer F, Nusser M, Brenner‐weiß G, Sedghamiz E, Wenzel W, Mittmann E, Rabe KS, Niemeyer CM, Franzreb M, Wöll C. In MOF eingebettete Enzyme für die kontinuierliche Durchflusskatalyse in wässrigen und organischen Lösungsmitteln. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202117144] [Reference Citation Analysis]
18 Bierbaumer S, Schmermund L, List A, Winkler CK, Glueck SM, Kroutil W. Synthesis of Enantiopure Sulfoxides by Concurrent Photocatalytic Oxidation and Biocatalytic Reduction. Angewandte Chemie. [DOI: 10.1002/ange.202117103] [Reference Citation Analysis]
19 Alcántara AR, Domínguez de María P, Littlechild JA, Schürmann M, Sheldon RA, Wohlgemuth R. Biocatalysis as Key to Sustainable Industrial Chemistry. ChemSusChem 2022;:e202102709. [PMID: 35238475 DOI: 10.1002/cssc.202102709] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
20 Pérez‐martín C, Rebolledo F, Brieva R. Amine Transaminase Mediated Synthesis of Optically Pure Piperazinones and 1,4‐Diazepanones. Adv Synth Catal 2022;364:1326-36. [DOI: 10.1002/adsc.202101510] [Reference Citation Analysis]
21 Benamara NE, Merabet‐khelassi M, Lakoud SG, Aribi‐zouioueche L, Riant O. Enantioselective Enzymatic Synthesis of ( R )‐Phenyl Alkyl Esters and Their Analogue Amides using Fatty Acids as Green Acyl Donors. ChemistrySelect 2021;6:13941-6. [DOI: 10.1002/slct.202103831] [Reference Citation Analysis]
22 Oroz‐guinea I, Winkler CK, Glueck SM, Ditrich K, Weingarten M, Breuer M, Schachtschabel D, Kroutil W. Ene‐Reductase Catalyzed Regio‐ and Stereoselective 1,4‐Mono‐Reduction of Pseudoionone to Geranylacetone. ChemCatChem. [DOI: 10.1002/cctc.202101557] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
23 Juma WP, Nyoni D, Brady D, Bode ML. The Application of Biocatalysis in the Preparation and Resolution of Morita-Baylis-Hillman Adducts and Their Derivatives. Chembiochem 2021. [PMID: 34822736 DOI: 10.1002/cbic.202100527] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Ospina F, Schülke KH, Hammer SC. Biocatalytic Alkylation Chemistry: Building Molecular Complexity with High Selectivity. Chempluschem 2021. [PMID: 34821073 DOI: 10.1002/cplu.202100454] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
25 Citoler J, Finnigan W, Bevinakatti H, Turner NJ. Direct Enzymatic Synthesis of Fatty Amines from Renewable Triglycerides and Oils. Chembiochem 2021. [PMID: 34726829 DOI: 10.1002/cbic.202100578] [Reference Citation Analysis]
26 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: 5.0] [Reference Citation Analysis]
27 Schneider P, Henßen B, Paschold B, Chapple BP, Schatton M, Seebeck FP, Classen T, Pietruszka J. Biocatalytic C3-Indole Methylation-A Useful Tool for the Natural-Product-Inspired Stereoselective Synthesis of Pyrroloindoles. Angew Chem Int Ed Engl 2021;60:23412-8. [PMID: 34399441 DOI: 10.1002/anie.202107619] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 10.0] [Reference Citation Analysis]
28 Klaus M, Zurek PJ, Kaminski TS, Pushpanath A, Neufeld K, Hollfelder F. Ultrahigh-Throughput Detection of Enzymatic Alcohol Dehydrogenase Activity in Microfluidic Droplets with a Direct Fluorogenic Assay. Chembiochem 2021. [PMID: 34643305 DOI: 10.1002/cbic.202100322] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Hu H, Wang Q, Wang D, Ao Y. Modification of the Enantioselectivity of Biocatalytic meso ‐Desymmetrization for Synthesis of Both Enantiomers of cis ‐1,2‐Disubstituted Cyclohexane by Amidase Engineering. Adv Synth Catal 2021;363:4538-43. [DOI: 10.1002/adsc.202100597] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
30 Schneider P, Henßen B, Paschold B, Chapple BP, Schatton M, Seebeck FP, Classen T, Pietruszka J. Biokatalytische C3‐Indol‐Methylierung – ein nützliches Werkzeug für die naturstoffinspirierte stereoselektive Synthese von Pyrroloindolen. Angew Chem 2021;133:23600-6. [DOI: 10.1002/ange.202107619] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
31 Biermann U, Bornscheuer UT, Feussner I, Meier MAR, Metzger JO. Fettsäuren und Fettsäurederivate als nachwachsende Plattformmoleküle für die chemische Industrie. Angewandte Chemie 2021;133:20304-20326. [DOI: 10.1002/ange.202100778] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
32 Li F, Yang L, Zhang J, Chen JS, Renata H. Stereoselective Synthesis of β‐Branched Aromatic α‐Amino Acids by Biocatalytic Dynamic Kinetic Resolution**. Angew Chem 2021;133:17821-6. [DOI: 10.1002/ange.202105656] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
33 Tang Q, Pavlidis IV, Badenhorst CPS, Bornscheuer UT. From Natural Methylation to Versatile Alkylations Using Halide Methyltransferases. Chembiochem 2021;22:2584-90. [PMID: 33890381 DOI: 10.1002/cbic.202100153] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
34 Li Z, Yang H, Liu J, Huang Z, Chen F. Application of Ketoreductase in Asymmetric Synthesis of Pharmaceuticals and Bioactive Molecules: An Update (2018-2020). Chem Rec 2021;21:1611-30. [PMID: 33835705 DOI: 10.1002/tcr.202100062] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 13.0] [Reference Citation Analysis]
35 Sun Z, Zhao Q, Haag R, Wu C. Responsive Emulsions for Sequential Multienzyme Cascades. Angew Chem 2021;133:8491-8495. [DOI: 10.1002/ange.202013737] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
36 Romero E, Jones BS, Hogg BN, Rué Casamajo A, Hayes MA, Flitsch SL, Turner NJ, Schnepel C. Enzymkatalysierte späte Modifizierungen: Besser spät als nie. Angew Chem 2021;133:16962-93. [DOI: 10.1002/ange.202014931] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]