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Cornerstones in Contemporary Inorganic Chemistry
Cornerstones in Contemporary Inorganic Chemistry
Autore Gregory Duncan
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (342 p.)
Soggetto topico Research & information: general
Chemistry
Inorganic chemistry
Soggetto non controllato cyanoguanidine
silver
crystal structure
chemical bonding
CuII
pyridine amides
pyrazine amide
amino benzamides
EPR spectroscopy
lanthanides
Schiff base
synthetic strategies
single-molecule magnets
Atomic Layer Deposition
Ni catalyst
reforming catalyst
thermodynamics
metallopharmaceuticals
cancer stem cells
copper
bioinorganic chemistry
medicinal inorganic chemistry
reactive oxygen species
metal-carbonyl complexes
[FeFe]-hydrogenases
density functional theory
time-dependent DFT
organometallic photochemistry
crystalline borosilicate
actinides
supercritical hydrothermal synthesis
waste forms
thorium
rhenium
ruthenium
metal-metal bonds
uranium
ceria
hydrothermal
catalysis
nanomaterials
crystallisation
4,2':6',4"-terpyridine
3,2':6',3"-terpyridine
coordination polymer
isomers
lithium
potassium
Nacnac
β-diketiminate
tricyclohexylphenyl
steric bulk
silver complexes
permanganates
perchlorates
perrhenate
pyridine
structure
spectroscopy
thermal behavior
heterogenous catalyst
metal-organic framework (MOF)
olefin epoxidation
carbon dioxide cycloaddition
f-element
lanthanide
actinide
multidentate ligand
macrocycle
ammonothermal synthesis
fluoride
aluminum
speciation
equilibria
thermodynamic stability
peptides
multivariate linear regression
poisoning effect of polar monomers
Brookhart-type catalysts
Zintl clusters
X-ray crystallography
Density Functional Theory
ISBN 3-0365-5705-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910674373303321
Gregory Duncan  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
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