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