Biocatalytic Process Optimization |
Autore | Kuo Chia-Hung |
Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
Descrizione fisica | 1 electronic resource (296 p.) |
Soggetto topico | Research & information: general |
Soggetto non controllato |
catechin
degalloylation flavonol glycoside hydrolase optimization tannase immobilized DERA statin side chain continuous flow synthesis alginate-luffa matrix design of experiments Anguilla marmorata eel protein hydrolysates functional properties herbal eel extracts agarose agarase agarotriose agaropentaose expression calycosin calycosin-7-O-β-D-glucoside glucosyltransferase sucrose synthase UDP-glucose recycle UGT-SuSy cascade reaction Candida antarctica lipase A surface-display system shear rate mass transfer rate enzymatic kinetic study enzymatic synthesis β-amino acid esters microreactor aromatic amines Michael addition kraft pulp cellulose xylan enzymatic hydrolysis Penicillium verruculosum glucose xylose lipase acidolysis docosahexaenoic acid ethyl ester eicosapentaenoic acid ethyl ester ethyl acetate kinetics styrene monooxygenase indole monooxygenase two-component system chiral biocatalyst solvent tolerance biotransformation epoxidation NAD(P)H-mimics superoxide dismutase (SOD) catalase (CAT) glutathione reductase (GR) aluminum (Al) selenium (Se) mouse brain liver phosphatidylcholine 3,4-dimethoxycinnamic acid enzymatic interesterification biocatalysis Pleurotus ostreatus enenzymatic hydrolysis peptide antioxidant hepatoprotective activity Yarrowia lipolytica whole-cell biocatalysis indolizine cycloaddition trehalose viscosity enzymes protein dynamics Kramers' theory protein stabilization enzyme inhibition Lipase transesterification 2-phenylethyl acetate packed-bed reactor solvent-free cyclic voltammetry electrochemical impedance spectroscopy carbon nanotubes redox mediators CYP102A1 naringin dihydrochalcone neoeriocitrin dihydrochalcone regioselective hydroxylation |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910557487503321 |
Kuo Chia-Hung | ||
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Carotenoids |
Autore | Sliwka Hans-Richard |
Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
Descrizione fisica | 1 electronic resource (168 p.) |
Soggetto non controllato |
singlet-triplet annihilation
silicon carotenoids dye-sensitized solar cells spent coffee grounds astaxanthin antioxidant antagonism carotenoid and chlorophyll derivatives fluorocarotenoids RNS feed processing ?-carotene iodocarotenoids hydrophilic selenium carotenoids free radical kinetics mechanisms stability free radicals antioxidant soil amendment pressurized fluid extraction extraction metal ions lutein lettuce lycopene antioxidant synergism iron carotenoids ROS solubility flavonoids bromocarotenoids sulfur carotenoids marine carotenoids cationic lipid carotenoids antioxidants nelfinavir fruit SK-Hep-1 carotenoid storage vegetables ethanol exon skipping inflammation xanthophylls Duchenne muscular dystrophy pharmacokinetics carrots chlorocarotenoids chelating compound cardiovascular disease ageing accelerated solvent extraction nitrogen carotenoids VEGF chlorophyll liquid chromatography antiradical PEG conjugates injection solvent cycloaddition HIV esterification antisense oligonucleotide B16F10 interaction cancer chemoprevention antireductant PC-3 oxidative stress |
ISBN | 3-03921-865-4 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910367739703321 |
Sliwka Hans-Richard | ||
MDPI - Multidisciplinary Digital Publishing Institute, 2019 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
New Trends in Catalysis for Sustainable CO2 Conversion |
Autore | Ereña Loizaga Javier |
Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
Descrizione fisica | 1 electronic resource (294 p.) |
Soggetto topico |
Technology: general issues
History of engineering & technology Environmental science, engineering & technology |
Soggetto non controllato |
carbon dioxide
hydrogenation catalyst gas hourly space velocity (GHSV) fixed-bed reactor CO2-H2O photo-co-processing VIS-light driven reactions CO2 reduction photocatalysts properties soft oxidant oxidation dehydrogenation nano-catalyst electrochemical reduction of CO2 ionic liquids propylene carbonate imidazolium cation greenhouse gas climate change CO2 decomposition CO2 utilization SrFeO3−x CO2 methanation Ni-xSi/ZrO2 Si promotion oxygen vacancies CO2 hydrogenation light olefins catalyst deactivation CO2-Fischer-Tropsch (CO2-FT) iron-based catalysts methanol to olefins bifunctional composite catalysts SAPO-34 photocatalysis carbon-TiO2 nanocarbon carbon allotropes carbon nanotubes carbon nanofibers carbon nano-onions carbon dioxide electrolysis molten carbonate greenhouse gas mitigation cycloaddition ionic liquid deep eutectic solvents onium salt homogeneous catalysts heterogeneous catalysis CO2 conversion methane hydrocarbons iron oxide copper nanoparticles biomass Fischer-Tropsch synthesis carbon-supported iron catalyst gasoline diesel |
ISBN | 3-0365-5912-4 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910640000303321 |
Ereña Loizaga Javier | ||
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Nitro Compounds and Their Derivatives in Organic Synthesis |
Autore | Nishiwaki Nagatoshi |
Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
Descrizione fisica | 1 electronic resource (120 p.) |
Soggetto topico | Research & information: general |
Soggetto non controllato |
nitro
pyridone 1-methyl-2-quinolone cycloaddition direct functionalization perylenediimide nitro group organic materials Phenacylation of beta-nitropyridin-2-ones 8-nitro-5-RO-indolizines oxazole-pyrrole ring transformation conjugate addition dihydrofuran 1,3-dicarbonyl compound enolate isoxazoline N-oxide nitroketone nitronate nucleophilic substitution nitropyridines isoxazolo[4,3-b]pyridines 1,4-dihydropyridines nucleophilic addition Diels-Alder reaction dearomatization hexapyrrolohexaazacoronene nitration SNAr substitution ICT character aromaticity C–H functionalization total synthesis pyrrolidines anchimeric assistance epimerization PDE4 inhibitors 1,3-Dipole electron-withdrawing ability electrophilicity nucleophilicity |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910557494003321 |
Nishiwaki Nagatoshi | ||
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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