| Nome |
# |
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Direct conversion of polyconjugated compounds into their corresponding carboxylic acids by Acetobacter aceti, file dfa8b990-0eb7-748b-e053-3a05fe0a3a96
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398
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Simple 1,3-diamines and their application as ligands in ruthenium(ii) catalysts for asymmetric transfer hydrogenation of aryl ketones, file dfa8b992-3ac6-748b-e053-3a05fe0a3a96
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372
|
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Production of optically pure molecules by asymmetric reductions with yeasts, file dfa8b98f-2a79-748b-e053-3a05fe0a3a96
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345
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Efficient methodology to produce a duloxetine precursor using whole cells of Rhodotorula rubra, file dfa8b995-98a3-748b-e053-3a05fe0a3a96
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314
|
|
Synthesis and biological evaluation of new natural phenolic (2E,4E,6E)-Octa-2,4,6-trienoic esters, file dfa8b99b-68ac-748b-e053-3a05fe0a3a96
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274
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Alternative Strategy to Obtain Artificial Imine Reductase by Exploiting Vancomycin/D-Ala-D-Ala Interactions with an Iridium Metal Complex, file dfa8b9a5-aace-748b-e053-3a05fe0a3a96
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235
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Ruthenium(II) complexes bearing (NNN) ligand : catalytic evaluation of different solvent-mediated coordination modes, file dfa8b99b-3bdf-748b-e053-3a05fe0a3a96
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208
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Evaluation of chemical diversity of biotinylated chiral 1,3-diamines as a catalytic moiety in artificial imine reductase, file dfa8b995-7a00-748b-e053-3a05fe0a3a96
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202
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Ctr-1 Mets7 motif inspiring new peptide ligands for Cu(i)-catalyzed asymmetric Henry reactions under green conditions, file dfa8b995-abd0-748b-e053-3a05fe0a3a96
|
185
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Cascade Reaction by Chemo- and Biocatalytic Approaches to Obtain Chiral Hydroxy Ketones and anti 1,3-Diols, file dfa8b99b-3fa0-748b-e053-3a05fe0a3a96
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158
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Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction, file dfa8b99f-51bc-748b-e053-3a05fe0a3a96
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97
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New insights into glycopeptide antibiotic binding to cell wall precursors using SPR and NMR spectroscopy, file dfa8b99c-bc7e-748b-e053-3a05fe0a3a96
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92
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Continuous-flow stereoselective reduction of prochiral ketones in a whole cell bioreactor with natural deep eutectic solvents, file dfa8b9a9-de55-748b-e053-3a05fe0a3a96
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62
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Self-assembly of an amphipathic ααβ-tripeptide into cationic spherical particles for intracellular delivery, file dfa8b99b-89c8-748b-e053-3a05fe0a3a96
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60
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Production of fructooligosaccharides by mycelium-bound transfructosylation activity present in Cladosporium cladosporioides and Penicilium sizovae, file dfa8b99c-bfa9-748b-e053-3a05fe0a3a96
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54
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Ni²⁺ and Cu²⁺ Biosorption by EPS-Producing Serratia plymuthica Strains and Potential Bio-Catalysis of the Organo–Metal Complexes, file b27bc8f5-8ec5-4796-8699-f619b41450d4
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41
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Hybrid Catalysts from Copper Biosorbing Bacterial Strains and Their Recycling for Catalytic Application in the Asymmetric Addition Reaction of B2(pin)2 on α,β-Unsaturated Chalcones, file dfa8b9aa-3aa1-748b-e053-3a05fe0a3a96
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36
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Combined chemical and biocatalytic approach for asymmetric one-pot reactions, file a8c096ae-fe9a-4a43-b367-9c0c8b85e659
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28
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Ctr-1 Mets7 motif inspiring new peptide ligands for Cu(i)-catalyzed asymmetric Henry reactions under green conditions, file dfa8b99c-cf07-748b-e053-3a05fe0a3a96
|
26
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Recycling of copper contaminants from wastewater as new hybrid catalysts for the synthesis of valuable pharmaceutical intermediates, file 434f3d90-570f-4d66-b21f-38c17868c306
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24
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Chemoenzymatic approach towards the synthesis of the antitumor and antileishmanial marine metabolite (+)-Harzialactone A via the stereoselective, biocatalyzed reduction of a prochiral ketone, file f563946a-77d3-485e-94b6-3898e77fe923
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21
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Catalytic Applications for Heavy Metals Bio-recovery, file dfa8b9a9-55ed-748b-e053-3a05fe0a3a96
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19
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Asymmetric one-pot reaction matching chemical and biocatalytic approaches, file 49dcb60b-2548-404e-b7b9-38c11b42f4a6
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14
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One-pot reactions in catalysis: a valuable tool for the synthesis of enantiopure intermediates for pharmaceutical applications, file e1133b06-57dd-48fc-a2a3-3f067fa7de12
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10
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Preparation of enantiomerically enriched aromatic β-hydroxynitriles and halohydrins by ketone reduction with recombinant ketoreductase KRED1-Pglu, file dfa8b99b-8306-748b-e053-3a05fe0a3a96
|
9
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Ctr-1 Mets7 motif inspiring new peptide ligands for Cu(i)-catalyzed asymmetric Henry reactions under green conditions, file bc3cca0d-017b-47f2-a0bc-6622d84e979f
|
8
|
|
Efficient methodology to produce a duloxetine precursor using whole cells of Rhodotorula rubra, file dfa8b99c-e695-748b-e053-3a05fe0a3a96
|
7
|
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Cytotoxic effect of (1-methyl-1H-imidazol-2-yl)-methanamine and its derivatives in PtII complexes on human carcinoma cell lines: A comparative study with cisplatin, file dfa8b990-8ed2-748b-e053-3a05fe0a3a96
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6
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Enzymatic hydrolysis of capsaicins for the production of vanillylamine using ECB deacylase from Actinoplanes utahensis, file dfa8b993-b41e-748b-e053-3a05fe0a3a96
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6
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Preparation of enantiomerically enriched aromatic β-hydroxynitriles and halohydrins by ketone reduction with recombinant ketoreductase KRED1-Pglu, file dfa8b99c-98dc-748b-e053-3a05fe0a3a96
|
6
|
|
Production of fructooligosaccharides by mycelium-bound transfructosylation activity present in Cladosporium cladosporioides and Penicilium sizovae, file dfa8b994-7c6e-748b-e053-3a05fe0a3a96
|
5
|
|
Ruthenium(II) complexes bearing (NNN) ligand : catalytic evaluation of different solvent-mediated coordination modes, file dfa8b99c-9c57-748b-e053-3a05fe0a3a96
|
4
|
|
Biotrasformation of Lipoglycopeptides, file dfa8b98f-f0bd-748b-e053-3a05fe0a3a96
|
3
|
|
New insights into glycopeptide antibiotic binding to cell wall precursors using SPR and NMR spectroscopy, file dfa8b993-7281-748b-e053-3a05fe0a3a96
|
3
|
|
8-Amino-5,6,7,8-tetrahydroquinolines as ligands in iridium(III) catalysts for the reduction of aryl ketones by asymmetric transfer hydrogenation (ATH), file dfa8b993-c4bd-748b-e053-3a05fe0a3a96
|
3
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|
Self-assembly of an amphipathic ααβ-tripeptide into cationic spherical particles for intracellular delivery, file dfa8b999-a684-748b-e053-3a05fe0a3a96
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3
|
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Chemoenzymatic deacylation of ramoplanin, file dfa8b993-6993-748b-e053-3a05fe0a3a96
|
2
|
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Biotransformation of aromatic ketones and ketoesters with the non-conventional yeast Pichia glucozyma, file dfa8b993-9cd3-748b-e053-3a05fe0a3a96
|
2
|
|
New Mets7 motif metallopeptide catalysts for Cu(I)-catalyzed asymmetric Henry reaction, file dfa8b998-5d11-748b-e053-3a05fe0a3a96
|
2
|
|
Evaluation of chemical diversity of biotinylated chiral 1,3-diamines as a catalytic moiety in artificial imine reductase, file dfa8b9a1-1495-748b-e053-3a05fe0a3a96
|
2
|
|
New antiproliferative platinum(II) complexes based on imidazol moiety, file dfa8b992-8eeb-748b-e053-3a05fe0a3a96
|
1
|
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3-(Hydroxy(phenyl)methyl)azetidin-2-ones obtained via catalytic asymmetric hydrogenation or by biotransformation, file dfa8b992-c3be-748b-e053-3a05fe0a3a96
|
1
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Enantioselective reduction and deracemisation using the non-conventional yeast Pichia glucozyma in water-organic solvent biphasic systems : preparation of (S)-1,2-diaryl-2-hydroxyethanones (benzoins), file dfa8b993-9afe-748b-e053-3a05fe0a3a96
|
1
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Chemo- and biocatalytic strategies to obtain phenylisoserine, lateral chain of taxol by asymmetric reduction, file dfa8b993-9d3d-748b-e053-3a05fe0a3a96
|
1
|
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Mets7 motif peptides in coordinative Cu(I) complexes: application in asymmetric Henry reaction, file dfa8b998-5d0f-748b-e053-3a05fe0a3a96
|
1
|
|
Conventional and non-conventional catalytic systems for the asymmetric reduction of cyclic imines, file dfa8b99c-0553-748b-e053-3a05fe0a3a96
|
1
|
|
Synthesis and biological evaluation of new natural phenolic (2E,4E,6E)-Octa-2,4,6-trienoic esters, file dfa8b99c-32d6-748b-e053-3a05fe0a3a96
|
1
|
|
Biotransformation of aromatic ketones and ketoesters with the non-conventional yeast Pichia glucozyma, file dfa8b99c-bf9d-748b-e053-3a05fe0a3a96
|
1
|
|
Dynamic kinetic resolution of calchones by chemo- and bio-catalytic approach, file dfa8b9a3-092c-748b-e053-3a05fe0a3a96
|
1
|
|
Vancomycin/D-Ala-D-Ala interaction: a new strategy to obtain artificial imine reductases, file dfa8b9a3-4673-748b-e053-3a05fe0a3a96
|
1
|
|
Alternative Strategy to Obtain Artificial Imine Reductase by Exploiting Vancomycin/D-Ala-D-Ala Interactions with an Iridium Metal Complex, file dfa8b9a6-c2e5-748b-e053-3a05fe0a3a96
|
1
|
| Totale |
3.357 |