top

  Info

  • Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.
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
Opac: Controlla la disponibilità qui
Recent Advances in Iron Catalysis
Recent Advances in Iron Catalysis
Autore Knölker Hans-Joachim
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (224 p.)
Soggetto topico Research & information: general
Soggetto non controllato alcohols
aldehyde
alkenyl halides
alkylation
amidation
amides
amines
aryl esters
asymmetric catalysis
asymmetric transfer hydrogenation
ate iron(II) complex
ATRP
bifunctional catalyst
BINOL synthesis
bis-(aryl)manganese
borylation
C-C coupling
C-H activation
C-H functionalisation
C-H functionalization
C-O activation
carbene
carboazidation
catalysis
cinnamamide
controlled radical polymerization
cross-coupling
decarbonylation
dehydrogenative coupling
density functional theory
DFT
diazoalkane
esters
external stimuli
Fe-catalysis
FeI/FeII/FeIII mechanism
fluorescence
Grignard reagent
haloalkane coupling
hydrogen transfer
iron
Iron
iron catalysis
iron catalyst
iron complexes
iron-catalysis
iron(III) chloride
Kumada cross-coupling
naphthidines
nitrogen ligand
organic synthesis
oxidative coupling
photochemistry
pinacolborane
radical
reductive amination
solvent-free
spirocyclization
sustainability
α-alkenylation
β-methyl scission
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557556003321
Knölker Hans-Joachim  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui