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Catalytic Transformation of Renewables (Olefin, Bio-sourced, et. al)
Catalytic Transformation of Renewables (Olefin, Bio-sourced, et. al)
Autore Dimitratos Nikolaos
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (248 p.)
Soggetto topico Research & information: general
Technology: general issues
Soggetto non controllato 2 methyl-furan
2,5-furandicarboxylic acid
5-(hydroxymethyl)furfural
ab initio
acid-base characterization
adiabatic reactor
alkylation
base-free
bimetallic nanoparticles
bio-based platform chemicals
biocatalysis
biomass
biomass conversion
capping agent
catalysis
catalyst design
catalytic hydrogen transfer reduction
cellobiose
chemical modification
Co/SBA-15
colloidal synthesis
cross-flow autohydrolysis
diffusion
dry gel conversion
embedded catalysts
Eucalyptus globulus wood
Fischer-Tropsch synthesis
furan-2-acrolein
furans
furfural
furoic acid
glucose
glycosidation
gold
gold catalysis
green oxidation
H-ZSM-5
hemicellulose-derived products
HMF
hydrodeoxygenation
hydrogenation
hydrolytic hydrogenation
hydrotalcite
in-situ synthesis
industrial design
iron
isomorphous substitution
kinetic modeling
magnesium oxide
MCM-41
methanol
methylbutynol test reaction
MFI zeolite
MPV reaction
multiscale modeling
n/a
nanoparticles
nickel phosphide
oxidation
oxidative condensation
palladium
particle size
particle sizes
Pd-based catalysts
pore length
pore size
reduction
selective oxidation
silica sources
Sn-Beta zeolite
sol-immobilization
solid acid
solid base
sorbitol
whole cells
zeolite catalysis
zeolites
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Catalytic Transformation of Renewables
Record Nr. UNINA-9910557678203321
Dimitratos Nikolaos  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern Strategies for Heterocycle Synthesis
Modern Strategies for Heterocycle Synthesis
Autore Favi Gianfranco
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (372 p.)
Soggetto topico Medicine
Soggetto non controllato 1-oxa-triene
1,2,3-triazol
1,3-oxazines
1H-imidazole-2(3H)-thione
2H-imidazo[2,1-b][1,3,4]thiadiazine
2H-pyran
3-trifluoroacetyl coumarins
3,2':6',3"-terpyridine
4-bromo quinolines
5-acylamino-1,3-thiazoles
acylhydrazone group
alkynes
alkynoic acids
amine nucleophiles
antifungal activities
antitumor
aromatic substitution
arylation
asymmetric dimeric β-carboline
aza-Wittig
azides
cascade cyclization
cascade reaction
CF3CO-acetylenes
cinnolines
click reaction
condensation
copper-catalyzed azide-alkyne cycloaddition
coumarin
CuAAC
cyclic ethers
cycloalkynes
cyclohexanol derivative
cycloisomerization
cytotoxic
cytotoxicity
dienone
dihydrocoumarins
enol ethers
fluorescence
fluorinated heterocycles
fluoroalcohol
fused N-heterocycles
gold catalysis
Hantzsch reaction
heterocycles
heterocyclic
inter-molecular approach
intra-molecular approach
ketone
Knoevenagel
multicomponent reaction
multicomponent reactions
n/a
natural products
nucleobase
organic dyes
organocatalysis
oxa-electrocyclization
phenols
photocatalysis
photoredox
photoredox cyclization
propargyl Claisen
propargylic alcohols
purine
pyrazolo[3,4-b]pyridine
pyridine
pyrrolidones
Richter cyclization
saturated oxygen heterocycles
silica sulfuric acid
solid-phase synthesis
Staudinger reaction
structure-activity relationship
Suzuki coupling
synthesis
synthesis of benzofurans
terpyridines
TMSBr
total synthesis
traceless synthesis
triazoles
triazolylmethyl phosphate
triazolylmethyl phosphinate
valence isomerism
visible-light-induced catalysis
α-chloroglycinates
α-halohydrazones
γ-lactam
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557409903321
Favi Gianfranco  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui