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Amide Bond Activation
Amide Bond Activation
Autore Szostak Michal
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (466 p.)
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 3-03921-204-4
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
Opac: Controlla la disponibilità qui
Anticancer Agents : Design, Synthesis and Evaluation
Anticancer Agents : Design, Synthesis and Evaluation
Autore Chen Qiao-Hong
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (606 p.)
Soggetto topico Medicine
Soggetto non controllato benzofurans
chemical synthesis
cytotoxic properties
HeLa
MOLT-4
K562
anticancer
anti-neuroinflammation
coumarin
dihydroartemisinin
flavonoids
allene
E-stereoselective
regioselective
anti-cancer activity
cyanopyridone
substituted pyridine
pyridotriazine
pyrazolopyridine
thioxotriazopyridine
anticancer activity
HepG2
antitumor activity
computational docking
MDM2-p53 interaction
xanthones
yeast-based assays
estrone derivatives
hydrazine
N-substituted pyrazoline
anti-ovarian cancer
topoisomerase II inhibitor
kinase inhibitor
antiproliferative agent
urea
synthesis
antiproliferative activity
apoptosis
indoleamine 2,3-dioxygenase
inhibitor
anti-tumor
immune modulation
tryptophan metabolism
taxoids
βIII-tubulin
P-glycoprotein
drug resistance
thiopene
thienopyrimidinone
thiazolidinone
breast cancer
benzofuran–pyrazole
nanoparticles
cytotoxic activity
PARP-1 inhibition
3,6-dibromocarbazole
5-bromoindole
carbazole
actin
migration
Thienopyrimidine
Pyrazole
PI3Kα inhibitor
quinazolin-4(3H)-one
quinazolin-4(3H)-thione
Schiff base
antioxidant activity
DFT study
ortho-quinones
beta-lapachone
tanshione IIA
PI3Ks
PI3Kδ inhibitors
2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide
anticancer agents
protein–protein interactions
virtual screening
mimetics
drug discovery
bivalency
polyvalency
antitumor
cell cycle
ovarian cancer
P-MAPA
IL-12
TLR signaling
inflammation
chemoresistance
4-(pyridin-4-yloxy)benzamide
1,2,3-triazole
c-Met
natural product
anticancer agent
zampanolide
Talazoparib
PARP inhibitor
prodrug
o-nitro-benzyl
photoactivatable protecting groups
salinomycin
overcoming drug resistance
tumor specificity
synergy
5-fluorouracil
gemcitabine
amides/esters
colchicine analogs
thiocolchicine
colchiceine
antimitotic agents
hydrates
dihydropyranoindole
HDAC inhibitors
neuroblastoma
aromatase
MCF-7
NIH3T3
benzimidazole
triazolothiadiazine
docking
ADME
organosilicon compounds
SILA-409 (Alis-409)
SILA-421 (Alis-421)
multidrug resistance (MDR) reversal
ABCB1 (P-glycoprotein)
colon cancer
colchicine amide
colchicine sulfonamide
tubulin inhibitors
docking studies
crystal structure
PROTACs
protein degradation
IGF-1R
Src
protein kinase
phenylpyrazolopyrimidine
enzyme inhibition
molecular simulation
androgen receptor
prostate cancer
enzalutamide
apalutamide
darolutamide
triple-negative breast cancer
cytotoxicity
chrysin analogues
flavonoid
anticancer compounds
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Anticancer Agents
Record Nr. UNINA-9910557129103321
Chen Qiao-Hong  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Pharmaceutical Crystals
Pharmaceutical Crystals
Autore Uekusa Hidehiro
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 electronic resource (148 p.)
Soggetto non controllato crystal structure analysis
famotidine
solution crystallization
salt optimization
structure determination from powder diffraction data
Hirshfeld surface analysis
DFT
molecular docking study
melting diagram
dehydration
hygroscopicity
HBV
Benzodioxole
pharmaceutical crystals
4-b]indol-4-one
pyrimidin-4(3H)-one
liquid assisted grinding
HOMO-LUMO
dissolution
cocrystal formation
Raman spectroscopy
carbamazepine
hydrogen bonding
3
ondansetron
physicochemical properties
solubility
succinic acid
cocrystal
adefovir dipivoxil
hepatitis B
polymorphs
hydrogen-bond-acceptance ability
DFT study
Nitrofurantoin-4-dimethylaminopyridine (NF-DMAP) salt
photostability
on-line monitoring
5-dihydro-4H-pyrimido[5
Imidazole
Semicarbazone
crystal habit
Crystal structure
solvent-mediated polymorphic transformation
ticagrelor
hydrate
pharmaceutical cocrystal
malonic acid
1H-indole
reactivity descriptors
famoxadone
crystal structure
dicarboxylic acid
hydrogen bond
saccharin
ISBN 3-03928-713-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910404091503321
Uekusa Hidehiro  
MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Removal of Organic Pollution in Water Environment
Removal of Organic Pollution in Water Environment
Autore Kotowska Urszula
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (154 p.)
Soggetto non controllato photodegradation
emerging organic contaminants
salicylic acid
biosorption
doxazosin maleate
boron-doped diamond electrode
sulfasalazine
continuous liquid–liquid extraction
water environment
electrochemical degradation
chlorinated intermediates
isotherm adsorption models
water
pollutants
sediment
ultrasound-assisted emulsification microextraction
emerging contaminants
electrochemical oxidation
selective sorbent
water remediation
HPLC-UV
sulfate radical
boron doped diamond
nickel aluminate
advanced oxidation processes
chemical oxygen demand
hormones
liquid-liquid continuous extraction
organic pollutant
run-off water
DFT study
biocides
DLLME-SFO
precious metals
budesonide
solidification of floating organic droplet
flame retardants
wastewater purification
graphene quantum dots
PBDE
disinfection by-products
1-undecanol
photocatalysis
total petroleum hydrocarbon
gas chromatography-mass spectrometry
EOCs determination
environmental samples
groundwater
fractional distillation
spinel
hydroxyl radical
removal of organic compounds
Guarani aquifer
density functional theory
persistent organic pollutants
hydroxyl radicals
ISBN 3-03921-841-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910674371803321
Kotowska Urszula  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
σ- and π-Hole Interactions
σ- and π-Hole Interactions
Autore Frontera Antonio
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (212 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato non-covalent interactions
regium bonds
silver(I)
coinage metals
pyrazolates
phosphines
halogen bonding
hydrogen bonding sigma-hole interactions
theoretical studies
characterizations
noncovalent interactions
Lewis acids
Lewis bases
spodium bonds
σ/π-hole interactions
EDTA
2,6-diaminopurine
cadmium
co-crystal
H-bonding
π–π stacking
triazinane
1,3,5-Triazacyclohexane
Hirshfeld surface analysis
DFT study
C–H···π interaction
hybridization of a nitrogen atom in sulfonamides
molecular cocrystal
sandwiched-layer structure
C–I···F halogen bonds
π···π stacking interactions
PBE0-D3(BJ) calculations
secondary bonding
supramolecular
crystal engineering
tetrel bonding
pnictogen bonding
chalcogen bonding
selenium
structural chemistry
main group elements
π–hole interaction
substituent effects
vibrational spectroscopy
local vibrational mode theory
direct measure for π–hole interaction strength
noncovalent interaction
hydrogen bonding
nickel
Schiff bases
crystallography
σ-hole
π-hole
crystal growth
supramolecular chemistry
σ-hole interactions
self-assembly
scanning tunneling microscopy
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557727903321
Frontera Antonio  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui