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Amide Bond Activation / Michal Szostak
Amide Bond Activation / Michal Szostak
Autore Szostak Michal
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (466 p.)
Soggetto topico Chemistry
Soggetto non controllato N-heterocyclic carbene
non planar amide
ruthenium (Ru)
physical organic chemistry
gemcitabine prodrug
pyramidal amides
bridged sultams
catalysis
dipeptides
N-(1-naphthyl)acetamide
C-N ? bond cleavage
steric effects
peptide bond cleavage
transition-metal-free
palladium
N-heterocyclic carbenes (NHCs)
addition reaction
C–O activation
rhodium
metal complexes
carbanions
thioamidation
amide bond
intramolecular catalysis
antiviral activity
additivity principle
pre-catalysts
C–N bond cleavage
bridged lactams
C–H acidity
arynes
twisted amides
organic synthesis
amination
Suzuki-Miyaura
tert-butyl
cyclopentadienyl complexes
C-S formation
enzymes
DFT study
sulfonamide bond
N
HERON reaction
primaquine
entropy
amide activation
amidation
synthesis
amide hydrolysis
carbonylicity
amide bond activation
amide bond resonance
aminosulfonylation
molecular dynamics
model compound
in situ
amide
homogeneous catalysis
heterocycles
anomeric effect
multi-component coupling reaction
kinetic
excited state
C–H bond cleavage
palladium catalysis
amides
thiourea
formylation
alkynes
cis/trans isomerization
amide C–N bond activation
intein
C-H functionalization
succindiamide
amide bonds
crown ether
aminoacylation
directing groups
cytostatic activity
reaction thermodynamics
acyl transfer
transition metals
N-dimethylformamide
DMAc
acylative cross-coupling
C-H/C-N activation
nickel catalysis
antibacterial screening
sodium
aryl thioamides
Winkler-Dunitz parameters
catalyst
N-dimethylacetamide
base-catalyed hydrolysis
nitrogen heterocycles
cross-coupling
insertion
amidicity
nitro-aci tautomerism
activation
carbonylation
transamidation
amine
distortion
Pd-catalysis
rotational barrier energy
hypersensitivity
N–C activation
metabolic stability
[2+2+2] annulation
twisted amide
protease
cyanation
amide resonance
trialkylborane
catalysts
biofilm eradication
pharmacokinetics
pancreatic cancer cells
DMF
aryl esters
Michael acceptor
fumardiamide
water solvation
ester bond activation
cyclization
nuclear magnetic resonance
secondary amides
reaction mechanism
density functional theory
density-functional theory
amino acid transporters
ISBN 9783039212040
3039212044
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346843703321
Szostak Michal  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Chiral Auxiliaries and Chirogenesis II
Chiral Auxiliaries and Chirogenesis II
Autore Borovkov Victor
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (160 p.)
Soggetto topico Research and information: general
Soggetto non controllato asymmetric synthesis
C-N bond formation
chiral ligands
chiral resolution
chirality
circular dichroism
circularly polarized luminescence
DFT
diffusion
enantiomeric analysis
enantioselective
exciton coupling
guanidine
heterocycles
host-guest binding
indole
induced optical activity
magnetochemistry
majority-rule
mirror symmetry breaking
molecular association
molecular chirality
multinuclear complexes
n/a
NMR
organocatalysis
paramagnetic NMR
parity violation
pillar[5]arene
planar chirality
polyfluorene
polyfluorenevinylene
polysilane
porphyrin
porphyrinoids
racemization kinetics
self-disproportionation of enantiomers (SDE)
self-induced diastereomeric anisochronism (SIDA)
sergeants-and-soldiers
stereodynamic chirality probe
supramolecular chemistry
TD-DFT simulation
transition-metal catalysis
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557757103321
Borovkov Victor  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Exclusive Feature Papers in Colorants
Exclusive Feature Papers in Colorants
Autore Prieto Jorge Bañuelos
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (156 p.)
Soggetto topico Technology: general issues
Soggetto non controllato 1,2-methyl orthoesters
2-arylazo-5-aryl-1,3,4-thiadiazoles
AIE
azo-coupling reactions
azobenzene
BODIPY
catalysis
colorant
crystal structure
d-d transition
dye
dye chemistry
electrochemistry
energy-electron transfer
environment-friendly
flavone
fluorescence
fluorescent labeling
fluorophore
glycosylation
heterocycles
inorganic pigments
membrane
Mn4+ ion
molecular rotors
morpholine
orange color
PI-88
polymeric blend
porphyrazine
solvatochromic probe
titanium(IV) oxide
tridentate ligand
viscosity sensors
zinc complex
zinc ion
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557375703321
Prieto Jorge Bañuelos  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Green Synthesis of Heterocycles
Green Synthesis of Heterocycles
Autore Arico Fabio
Pubbl/distr/stampa Frontiers Media SA, 2020
Descrizione fisica 1 online resource (95 p.)
Soggetto topico Science: general issues
Soggetto non controllato cyclic compound
green chemistry
green principles
heterocycles
sustainable
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557713003321
Arico Fabio  
Frontiers Media SA, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles
Autore Aronica Laura Antonella
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (124 p.)
Soggetto topico Chemistry
Organic chemistry
Research and information: general
Soggetto non controllato acyl radical
alkynes
carbonylation
catalyst recyclability
Cr-phthalocyanine
cyclisation
cyclopentenones
flow chemistry
Friedel-Crafts reaction
heterocycles
heterogeneous catalysis
Jaspine B
metal-mediated reactions
N-heterocycles
n/a
natural products total syntheses
O-heterocycles
palladium catalysis
Pauson-Khand reaction
porous organic polymer
radical carbonylation
silylcarbocyclization
silylformylation
visible light photocatalysis
β-lactones
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566464703321
Aronica Laura Antonella  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
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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
Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds
Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds
Autore Matiadis Dimitrios
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (124 p.)
Soggetto topico Research & information: general
Soggetto non controllato [1,3]-H shift
11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine
15N-NMR
4-anilino-quin(az)olines
alkyne
amino-substituted fused oxazolocoumarin
aminocyclopentitol
anion radical
Au-nanoparticles
aza-Michael addition
azopyridine
benzimidazole
bicyclic aziridine
bromination
C-C bond length
carbocyclic hydantoins
carbonyl complex
catechol
chalcogenophene
chemoselective reduction
chlorination
condensation
conformational flexibility
Cu(II) complex
curcuminoids
cytotoxic
DABCO
DFT calculations
dimethyl acetylenedicarboxylate
disulfur dichloride
DNA binding
domino reactions
electronic structure
fused oxazolocoumarins
gamma-amino acid
GIAO
heterocycle
heterocycles
hinge binder
homopiperazine
HRMS
imidazolidine-2,4-diones
imine
intramolecular SN displacement
isoxazolo[3,4-b]quinolin-3(1H)-one
kinase inhibitor design
ligands
magnetic properties
MDR reversal
N-1 substituted hydantoin
n/a
NaBH4
nitrogen heterocycles
NMR
nucleophilic aromatic substitution
nucleophilic displacement
nucleophilic substitution
o-aminophenol
o-hydroxynitrocoumarins
oxygen-nitrogen heterocycles
piperazine
pyrazolines
pyridine derivatives
pyrimidine
ring closing
ruthenium
Schiff base
spiro hydantoins
stereochemistry
thiol-alkyne click reaction
thiophene derivatives
thiosemicarbazone
water chemistry
X-ray crystallographic analysis
X-ray structure
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Nitrogen-Containing Molecules
Record Nr. UNINA-9910557605603321
Matiadis Dimitrios  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Organic Synthesis via Transition Metal-Catalysis
Organic Synthesis via Transition Metal-Catalysis
Autore Gabriele Bartolo
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (144 p.)
Soggetto topico Research & information: general
Soggetto non controllato palladium
indole
indomethacin
C-H functionalization
sulfoximide
C-H activation
benzothiazine
rhodium
catalysis
synthesis
organosulfur compounds
S-S bond cleavage
chemical equilibrium
reversible reaction
alkynes
annulation
benzimidazoxazinones
heterocycles
polycyclic heterocycles
heterocyclization
zinc
direct arylation
pincer complexes
vanadium(IV) complexes
biological activity
catalytic properties
8-hydroxyquinoline
cytotoxicity studies
hydroformylation
hydrogenation
tandem reaction
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557611103321
Gabriele Bartolo  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui