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For: Brenna E, Crotti M, Gatti FG, Manfredi A, Monti D, Parmeggiani F, Santangelo S, Zampieri D. Enantioselective Synthesis of ( R )-2-Arylpropanenitriles Catalysed by Ene-Reductases in Aqueous Media and in Biphasic Ionic Liquid-Water Systems. ChemCatChem 2014;6:2425-31. [DOI: 10.1002/cctc.201402205] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.1] [Reference Citation Analysis]
Number Citing Articles
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10 Prikhod'ko SA, Shabalin AY, Bardin VV, Eltsov IV, Shundrina IK, Parmon VN, Adonin NY. 1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties. RSC Adv 2017;7:17497-504. [DOI: 10.1039/c7ra01709j] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
11 Paula BRS, Zampieri D, Rodrigues JAR, Moran PJS. Bioreduction of α-Acetoxymethyl Enones: Proposal for an S N 2′ Mechanism Catalyzed by Enereductase. Adv Synth Catal 2016;358:3555-71. [DOI: 10.1002/adsc.201600601] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
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13 Brenna E, Crotti M, Gatti FG, Monti D, Parmeggiani F, Powell RW, Santangelo S, Stewart JD. Opposite Enantioselectivity in the Bioreduction of ( Z )-β-Aryl-β-cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to ( R )- and ( S )-β-Aryl-γ-lactams. Adv Synth Catal 2015;357:1849-60. [DOI: 10.1002/adsc.201500206] [Cited by in Crossref: 42] [Cited by in F6Publishing: 42] [Article Influence: 6.0] [Reference Citation Analysis]
14 Brenna E, Crotti M, Gatti FG, Monti D, Parmeggiani F, Pugliese A, Santangelo S. Multi-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesia®. Journal of Molecular Catalysis B: Enzymatic 2015;114:37-41. [DOI: 10.1016/j.molcatb.2014.10.006] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 2.4] [Reference Citation Analysis]