top

  Info

  • Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.
Biocatalytic Process Optimization
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
Opac: Controlla la disponibilità qui
Carotenoids
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
Opac: Controlla la disponibilità qui
New Trends in Catalysis for Sustainable CO2 Conversion
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
Opac: Controlla la disponibilità qui
Nitro Compounds and Their Derivatives in Organic Synthesis
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
Opac: Controlla la disponibilità qui