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Biocatalytic Process Optimization
Biocatalytic Process Optimization
Autore Kuo Chia-Hung
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (296 p.)
Soggetto topico Research & information: general
Soggetto non controllato 2-phenylethyl acetate
3,4-dimethoxycinnamic acid
acidolysis
agarase
agaropentaose
agarose
agarotriose
alginate-luffa matrix
aluminum (Al)
Anguilla marmorata
antioxidant
aromatic amines
biocatalysis
biotransformation
brain
calycosin
calycosin-7-O-β-D-glucoside
Candida antarctica lipase A
carbon nanotubes
catalase (CAT)
catechin
cellulose
chiral biocatalyst
continuous flow synthesis
cyclic voltammetry
cycloaddition
CYP102A1
degalloylation
design of experiments
docosahexaenoic acid ethyl ester
eel protein hydrolysates
eicosapentaenoic acid ethyl ester
electrochemical impedance spectroscopy
enenzymatic hydrolysis
enzymatic hydrolysis
enzymatic interesterification
enzymatic kinetic study
enzymatic synthesis
enzyme inhibition
enzymes
epoxidation
ethyl acetate
expression
flavonol
functional properties
glucose
glucosyltransferase
glutathione reductase (GR)
glycoside hydrolase
hepatoprotective activity
herbal eel extracts
immobilized DERA
indole monooxygenase
indolizine
kinetics
kraft pulp
Kramers' theory
lipase
Lipase
liver
mass transfer rate
Michael addition
microreactor
mouse
n/a
NAD(P)H-mimics
naringin dihydrochalcone
neoeriocitrin dihydrochalcone
optimization
packed-bed reactor
Penicillium verruculosum
peptide
phosphatidylcholine
Pleurotus ostreatus
protein dynamics
protein stabilization
redox mediators
regioselective hydroxylation
selenium (Se)
shear rate
solvent tolerance
solvent-free
statin side chain
styrene monooxygenase
sucrose synthase
superoxide dismutase (SOD)
surface-display system
tannase
transesterification
trehalose
two-component system
UDP-glucose recycle
UGT-SuSy cascade reaction
viscosity
whole-cell biocatalysis
xylan
xylose
Yarrowia lipolytica
β-amino acid esters
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
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Carotenoids
Carotenoids
Autore Sliwka Hans-Richard
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 online resource (168 p.)
Soggetto topico Biology, life sciences
Soggetto non controllato ?-carotene
accelerated solvent extraction
ageing
antioxidant
antioxidant antagonism
antioxidant synergism
antioxidants
antiradical
antireductant
antisense oligonucleotide
astaxanthin
B16F10
bromocarotenoids
cancer chemoprevention
cardiovascular disease
carotenoid
carotenoid and chlorophyll derivatives
carotenoids
carrots
cationic lipid
chelating compound
chlorocarotenoids
chlorophyll
cycloaddition
Duchenne muscular dystrophy
dye-sensitized solar cells
esterification
ethanol
exon skipping
extraction
feed processing
flavonoids
fluorocarotenoids
free radical kinetics
free radicals
fruit
HIV
hydrophilic
inflammation
injection solvent
interaction
iodocarotenoids
iron carotenoids
lettuce
liquid chromatography
lutein
lycopene
marine carotenoids
mechanisms
metal ions
nelfinavir
nitrogen carotenoids
oxidative stress
PC-3
PEG conjugates
pharmacokinetics
pressurized fluid extraction
RNS
ROS
selenium carotenoids
silicon carotenoids
singlet-triplet annihilation
SK-Hep-1
soil amendment
solubility
spent coffee grounds
stability
storage
sulfur carotenoids
vegetables
VEGF
xanthophylls
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 online resource (120 p.)
Soggetto topico Research & information: general
Soggetto non controllato 1-methyl-2-quinolone
1,3-dicarbonyl compound
1,3-Dipole
1,4-dihydropyridines
8-nitro-5-RO-indolizines
anchimeric assistance
aromaticity
C-H functionalization
conjugate addition
cycloaddition
dearomatization
Diels-Alder reaction
dihydrofuran
direct functionalization
electron-withdrawing ability
electrophilicity
enolate
epimerization
hexapyrrolohexaazacoronene
ICT character
isoxazoline N-oxide
isoxazolo[4,3-b]pyridines
nitration
nitro
nitro group
nitroketone
nitronate
nitropyridines
nucleophilic addition
nucleophilic substitution
nucleophilicity
organic materials
oxazole-pyrrole ring transformation
PDE4 inhibitors
perylenediimide
Phenacylation of beta-nitropyridin-2-ones
pyridone
pyrrolidines
SNAr substitution
total synthesis
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