- ISSN 0010-0765 printed
- ISSN 1212-6950 electronic
Keyword index
- C-Disaccharides
- C-Glycosides
- C-Nucleosides
- C2 Symmetry
- C2-Symmetric ligands
- C2-Symmetry
- C3 Symmetry
- Cameraria ohridella
- Candida antarctica lipase B
- Candida lusitaniae
- Candida mucifera
- Candida parapsilosis
- Candida albicans
- Candida tropicalis
- Candida sp. proteinases
- cap Analogs
- cis-Dinitrosylvanadium
- cis-Tetraazaperhydropyrene
- cis-[PtCl2(NH3)(2-picoline)]
- cis/trans Isomerism
- closo-1-Carbadodecaborate(1-) ion
- closo-Carborane
- closo-Decaborate
- closo-Decahydrodecaborate(2-)
- closo-Dodecaborate
- closo-Hydroborate anions
- Coxsackie virus
- Cydia molesta
- Cyprinus carpio
- C,N-chelates
- C,N-ligand
- C,N-ligands
- C-Branched nucleosides
- C-C bond formation
- C-C-Single bond activation
- C-H bond activation
- C2NO2 cation
- Cadmium
- Cadmium complexes
- Cadmium(II) complexes
- Caesium fluoroxysulfate
- Cage compounds
- Calcium
- Calcium oxide
- Calcium/cadmium formate double salt
- Calcium/cadmium formate mixed crystals
- Calculated log P values
- Calculations
- Calixarenes
- Calixpyrroles
- Calixpyrrols
- Calix[4]arenes
- Calix[8]arenes
- Caloric curves
- Calorimetry
- Camalexin
- cAMP
- Camphor
- Camphor dimers
- Camphor-derived ligands
- Camphorimine
- Cancer cells
- Cancer therapy
- Candesartan cilexetil
- Cannabinoids
- Cannizzaro reaction
- Canonical orthogonalization
- Capacitance
- Capacitance pit
- Capacity transients
- Capillary electrophoresis
- Capillary gas chromatography
- Capillary zone electrophoresis
- Capreomycidine
- Capreomycins
- Captopril
- Carba-analogues
- Carbaboranes
- Carbamates
- Carbanions
- Carbanucleosides
- Carbasugars
- Carbazole
- Carbazole energy donor
- Carbazoles
- Carbene complexes
- Carbenes
- Carbenoids
- Carbides
- Carbocation cyclizations
- Carbocations
- Carbocycles
- Carbocyclic
- Carbocyclic analogs
- Carbocyclic hexopyranoses
- Carbocyclic nucleosides
- Carbocyclic pentofuranoses
- Carbohydrate receptors
- Carbohydrate-binding protein
- Carbohydrates
- Carbometallation
- Carbon
- Carbon clusters
- Carbon dioxide
- Carbon dioxide fixation
- Carbon dioxide reduction
- Carbon electrode
- Carbon electrodes
- Carbon fibre microelectrode
- Carbon insertion
- Carbon monoxide
- Carbon monoxide chemisorption
- Carbon monoxides
- Carbon nanotube
- Carbon nanotubes
- Carbon nucleophiles
- Carbon paste
- Carbon paste electrode
- Carbon paste electrodes
- Carbon paste support
- Carbon rearrangement
- Carbon surface
- Carbon tetrachloride
- Carbonates, preparation by alkoxycarbonylation
- Carbonyl complexes
- Carbonyl compounds
- Carbonyl sulfide
- Carbonylation
- Carborane
- Carborane anions
- Carborane conjugates
- Carboranes
- Carboxamides
- Carboxylate binding
- Carboxylates
- Carboxylic acid
- Carboxylic acids
- Carboxypeptidase A
- Carcinogenesis
- Carcinogenity
- Carcinogens
- Cardenamides
- Cardenolides
- Cardiotonic
- Cardiovascular research
- Carmustine
- Carotenoids
- Carp
- Carp pituitary
- Carriers of medical drugs
- Cartesian components
- Carthamoside
- Carvone
- CAS reference
- CAS(n,m)CCSD
- Cascade cyclizations
- Cascade reactions
- CASPT2
- CASSCF
- CASSCF/CASPT2 method
- Cassiterite
- Catalases
- Catalysis
- Catalysis by metals
- Catalysis in water
- Catalysis on zeolites
- Catalysis with dyes
- Catalysis with sodium ion
- Catalyst
- Catalyst activity
- Catalyst deactivation
- Catalyst surface hydrophobicity
- Catalytic activity
- Catalytic combustion
- Catalytic currents
- Catalytic decomposition
- Catalytic electrooxidation
- Catalytic hydroboration
- Catalytic hydrogen evolution
- Catalytic hydrogen prewave
- Catalytic hydrogenation
- Catalytic hydroxylation
- Catalytic mechanism
- Catalytic oxidation
- Catalytic prewave
- Catalytic prewaves
- Catalytic properties
- Catalytic reductive carbonylation
- Catalytic removal of NO
- Catalytic wet oxidation
- Catechins
- Catecholamines
- Catecholborane
- Catenanes
- Cathodic activation
- Cathodic stripping voltammetry
- Cation exchanger
- Cation-radicals
- Cation-π interactions
- Cationic micelles
- Cationic polymerizations
- Cationic sites
- Cationic surfactant
- Cationic surfactants
- Cationic titanium complex
- Cations
- Cations in faujasites
- Cavitand
- Cavitands
- Cavitation
- Cavity correlations
- CCD camera
- CCSD
- CCSD(T)
- CCSD(T) method
- CCSDCT
- CD
- Cd complexes
- CD spectroscopy
- CDK Inhibitors
- CDOCKER
- Ce(III) ions
- Ce(IV) ions
- CeCl3·7H2O
- Cefetamet
- Cell
- Cell cycle
- Cell membrane models
- Cellulose
- Centrifugation
- CeO2-ZrO2
- Cephalosporins
- Cephalostatin
- Cephalostatin analogs
- Cephalostatin analogues
- Ceramic foam
- Ceric ammonium nitrate
- Cerium
- CESG
- Cesium
- Cesium cation
- Cesium salts
- Cetyltrimethylammonium bromide
- CGC catalysts
- Ch'an Su
- Chabazite
- Chalcone
- Chalcones
- Chaotic behaviour
- Chaperones
- Characterization procedure
- Charge capacity
- Charge distribution
- Charge profile
- Charge transfer
- Charge transfer characteristics
- Charge transfer coefficient
- Charge transfer complexes
- Charge-delocalized anions
- Charge-transfer complexes
- Charge-transfer interaction
- Charge-transfer interactions
- Charge-transfer potentiometry
- Charged osmotic brush
- Chelate ring formation
- Chelates
- Chelating ligands
- Chelating sorbents
- Chelilutine
- Chelirubine
- Chemical analysis
- Chemical biology
- Chemical communication
- Chemical equilibria
- Chemical equilibrium
- Chemical etching
- Chemical graphs
- Chemical kinetics
- Chemical modification
- Chemical oscillations
- Chemical oscillators
- Chemical oxygen-iodine laser
- Chemical potential
- Chemical reactor performance
- Chemical shift increments
- Chemical theory
- Chemical thermodynamics
- Chemical vapor deposition
- Chemically modified electrode
- Chemically modified electrodes
- Chemiluminescence
- Chemisorbed methylium cations
- Chemoenzymatic synthesis
- Chemometric
- Chemometrics
- Chemoselectivity
- Chemosensors
- Chemostat
- Chewing gum
- Chicken egg
- Chicken pituitary
- Chinese herbs nephropathy
- Chippiine/dippinine alkaloids
- Chiral
- Chiral alkenes
- Chiral analysis
- Chiral anion recognition
- Chiral auxiliaries
- Chiral bis(α-amino acid)s
- Chiral bis-anilines
- Chiral building blocks
- Chiral cavity
- Chiral clusters
- Chiral compounds
- Chiral crown compounds
- Chiral derivatizing agents
- Chiral diols
- Chiral discrimination
- Chiral ferrocenyldiphosphines
- Chiral forms
- Chiral HPLC
- Chiral intercalators
- Chiral ketones
- Chiral ligands
- Chiral nitrones
- Chiral phosphines
- Chiral pool
- Chiral porous solids
- Chiral reactions
- Chiral receptors
- Chiral recognition
- Chiral saturated heterocycles
- Chiral stationary phase
- Chiral stationary phases
- Chiral sulfoxides
- Chiral synthons
- Chirality
- Chloramine B
- Chloramphenicol
- Chloride bridges
- Chlorinated alcohols
- Chlorinated arenes
- Chlorinated compounds
- Chlorinated phenols
- Chlorination
- Chlorinations
- Chlorine-bridged complexes
- Chloro(phenyl)glyoxime complexes
- Chloroacetaldehyde
- Chloroalkanes
- Chloroalkenes
- Chlorobenzene
- Chlorodifluoromethyl
- Chlorofluoroalkyl iodides
- Chlorofluoroethenes
- Chloromethanes
- Chloronitrobenzenes
- Chlorophenols
- Chlorophenols electrooxidation
- Chlorophyll
- Cholesky decomposition
- Cholestane
- Cholesterol
- Cholesterol lowering agent
- Cholesterol mimics
- Cholinesterase
- Chromate and arsenate oxyanions
- Chromates
- Chromatographic separations
- Chromatography
- Chromenes
- Chromium
- Chromium (VI) oxide
- Chromium complexes
- Chromium fluoride
- Chromium fluorides
- Chromium hexacarbonyl
- Chromium oxide
- Chromium(VI) oxide
- Chromium(VI) toxicity
- Chronic hypoxia
- Chronoamperometry
- Chronopotentiometry
- Cidofovir
- Cinnamaldehyde
- Cinnamoyl derivatives
- Cinobufagin
- Circular dichroism
- Cisplatin
- Citrates
- Citrazinic acid
- CK2 inhibitors
- Claisen condensation
- Claisen rearrangement
- Claisen-Schmidt reactions
- Classical mechanics
- Clathrasil, isotherm
- Clathrate
- Clathrates
- Clathration
- Clavines
- Clays
- Clean fuel
- Cleavage
- Cleavage reactions
- Cleavamine
- Clerodone
- Click chemistry
- Clobetasone butyrate
- Closures
- Clothianidin
- Cluster
- Cluster bridging ligands
- Cluster chemistry: electron-counting considerations
- Cluster magic numbers
- Cluster method
- Cluster model calculations
- Cluster models
- Cluster opening
- Cluster stability
- Cluster-closure reactions
- Clusters
- CMO
- CN radical
- CO Adsorption
- Co complexes
- Co heteropolyoxomolybdate
- Co(II) ions
- Co(III) chelates
- Co(III) complexes
- Co-Beta
- Co-crystals
- Co-ferrierite
- Co-receptors
- Co-zeolite
- CO2 reduction
- CO2
- CO2-to-CO reduction
- Coal gas desulfurization
- Coalescence
- Coarsening
- Coating
- Cobalt
- Cobalt bis(dicarbollide) complexes
- Cobalt catalysis
- Cobalt clusters
- Cobalt complexes
- Cobalt oxinate
- Cobalt oxo compounds
- Cobalt phthalocyanine complexes
- Cobalt(II)
- Cobalt(II) complexes
- Cobalt(III) complexes
- Cobaltacarborane anion
- Cobaltacarborane sandwich complexes
- Cobaltacarborane with triatomic bridge
- Cobaltacarboranes
- Cobaltacarboranes with B-P terminal bonds
- Cobaltadicarbollides, bridged
- Cobalticarborane
- Cocaine
- CODESSA
- Coevolution
- Cohesion
- COIL
- Coinsertion tungsten bronzes
- Colchicine
- Colchicinoids
- Cold wall temperature effect
- Collision-induced dissociation
- Collisions
- Colloidal dispersions
- Colloidal particles
- Colloidal polyaniline composite suspension
- Colloidal silica density gradient
- Colloidal sulfur
- Colloidal zeolites
- Colloids
- Combinatorial chemistry
- Combinatorial libraries
- Combinatorial synthesis
- Combining rules
- CoMFA
- CoMo/Al2O3
- Competitive hydrogenation
- Competitive liquid extraction
- Complete active space
- Complete active space SCF
- Complete basis set
- Complete basis set extrapolations
- Complete basis set limit
- Complex formation
- Complex indole alkaloids
- Complex ions
- Complex mixtures
- Complex stability constants
- Complexation
- Complexes of aminoalkylphosphine oxides
- Complexes of Hg(II)
- Complexes of Schiff bases
- Complexes of substituted 2,2'-bipyridine
- Complexing agents
- Composite
- Composite materials
- Composition
- Comproportionation constant
- Computational approaches
- Computational chemistry
- Computer chemistry
- Computer simulation
- CoMSIA
- Concentration boundary layer
- Concentration polarisation
- Concerted mechanism
- Condensation in water
- Conductance
- Conductimetry
- Conducting materials
- Conducting polymer
- Conducting polymers
- Conductiong polymers
- Conductivity
- Conductometry
- Configuration
- Configuration energy
- Configuration interaction
- Confined quantum systems
- Confined systems
- Confining potential
- Conformation
- Conformation analysis
- Conformation equilibrium
- Conformation in water
- Conformation of nucleosides
- Conformational analysis
- Conformational behavior
- Conformational equilibria
- Conformational transitions
- Conformers
- Conical intersection
- Conical intersections
- Conical lens
- Conjugate additions
- Conjugated dienals
- Conjugated dienes
- Conjugated oligomers
- Conjugated polymers
- Conjugation
- Connecting bridge
- Connection formula
- Connectivity conditions
- Consistency
- Constant potential coulometry
- Constrained geometry complexes
- Contact value
- Contact value theorems
- Contactless conductivity detection
- Continuous stirred tank reactor
- Continuous-phase axial dispersion coefficient
- Control of chaos
- Controlled radical polymerizations
- Convergence
- Convergence of trajectory calculations
- Conversion
- Convolutamine F
- Convolutamine G
- Convolutamydine E
- Convolution-deconvolution voltammetry
- Cooperative effects
- Cooperativity
- Coordination
- Coordination chemistry
- Coordination complexes
- Coordination dendrimers
- Coordination number
- Coordination polymers
- Coordinative activation
- Cope rearrangement
- Copolymer micelles
- Copolymerizable UV stabilizer
- Copolymerization
- Copolymerizations
- Copolymers
- Copper
- Copper (II) chloride
- Copper alloys
- Copper catalysis
- Copper complexes
- Copper deposition
- Copper ligands
- Copper powder
- Copper protein
- Copper transport
- Copper(I) complexes
- Copper(I,II) cyanide
- Copper(II)
- Copper(II) chloride
- Copper(II) complexes
- Copper(II)-5,10,15,20-tetraphenylporphyrin
- Cordycepin
- Core interaction
- Core-electron process
- Core-shell model potential
- Coronene
- Correction for triples
- Correlated ab initio methods
- Correlation analysis
- Correlation effects
- Correlation energies
- Correlation energy
- Correlation functions
- Correlation of retention data and molecular weight
- Correlation-consistent bases
- Correlations
- Corrosion
- Corrosion resistivity
- Cosine coefficient
- COSMO
- Cottrell equation
- Coulomb forces
- Coulomb integrals
- Coulomb-type trial functions
- Coulombic forces
- Coulometric electrochemical and fluorescence detection
- Coulometry
- Coumarin
- Coumarins
- Counterpoise correction
- Counterpoise method
- Coupled cluster
- Coupled cluster calculations
- Coupled cluster method
- Coupled cluster methods
- Coupled clusters
- Coupled clusters linear response method
- Coupled-cluster
- Coupled-cluster calculations
- Coupled-cluster method
- Coupled-cluster methodology
- Coupled-cluster methods
- Coupling
- Coupling agents
- Coupling constant
- Coupling constants
- Coupling reactions
- CP compounds
- CP/MAS NMR spectroscopy, 13C and 119Sn
- cPrPMEDAP
- Cracking
- Crayfish
- Cresol
- Cris-cross cycloadditions
- Critical point
- Critical solution temperature
- Cross flow
- Cross-coupling
- Cross-coupling reactions
- Cross-dehydrocoupling polymerization
- Cross-interaction constants
- Cross-linked poly(ethylene glycol)
- Crossed-beam experiments
- Crosslinked poly(amide-imide)s
- Crosslinked polymers
- Crosslinking
- Crown compounds
- Crown ethers
- Cryolite
- Cryptands
- Cryptochirality
- Crystal and molecular structure
- Crystal engineering
- Crystal field potential
- Crystal forms
- Crystal growth
- Crystal growth rate
- Crystal orientation
- Crystal packing
- Crystal size and morphology
- Crystal structure
- Crystal structure determination
- Crystal structure reconstruction
- Crystal structures
- Crystallization
- Crystallizations
- Crystallizer dynamics
- Crystallography
- Crystals
- CT complex
- CT complexes
- Cu
- Cu ion
- Cu ion-exchanged molecular sieves
- Cu2+
- Cuckoo-bumblebees
- Cumulenes
- CuO
- Cuprates
- Curcumin
- Current efficiency
- Current oscillations
- Current transients
- Curtis macrocycle
- Curtius rearrangement
- Curved electrodes
- Cuticular hydrocarbons
- Cyanation
- Cyanide-bridged complexes
- Cyanides
- Cyanine
- Cyanine dyes
- Cyanoboranes
- Cyanodebromination
- Cyanoethyl protecting group
- Cyanoethylation
- Cyclam
- Cyclam cis-protection
- Cyclen
- Cyclen derivative
- Cyclic acetals
- Cyclic allyl alcohols
- Cyclic carbonates
- Cyclic chronopotentiometry
- Cyclic ketones
- Cyclic peptides
- Cyclic reciprocal derivative chronopotentiometry
- Cyclic sulfates
- Cyclic sulfites
- Cyclic voltammetry
- Cyclic voltammetry (CV)
- Cyclic voltammetry analysis
- Cycling behaviour
- Cycliosomerization
- Cyclisations
- Cyclitols
- Cyclization
- Cyclization involving nitro group
- Cyclization kinetics
- Cyclizations
- Cycloaddition
- Cycloaddition reactions
- Cycloadditions
- Cyclobutanes
- Cyclocondensation
- Cyclodextrins
- Cyclodimerization
- Cyclohexadienes
- Cyclohexanes
- Cyclohexanol dehydration
- Cyclohexene
- Cyclohexenones
- Cyclohexylation
- Cyclohexylnonadecanes
- Cycloisomerisation
- Cycloocta-1,5-diene complexes
- Cyclooctatetraene
- Cyclopentadiene
- Cyclopentadienes
- Cyclopentadienyl ligand
- Cyclopentadienyl ligands
- Cyclopentadienyltitanium(II) complexes
- Cyclopentane
- Cyclopentanes
- Cyclopentanones
- Cyclopentenes
- Cyclopentenones
- Cyclopentylicosane
- Cyclophane
- Cyclophanes
- Cyclophosphamide
- Cyclopropanation
- Cyclopropanes
- Cyclopropenes
- Cyclopropenones
- Cyclopropyl-allyl rearrangement
- Cyclosporin E
- Cyclosporins
- Cyclotrimerization
- Cyclotrimerizations
- Cyclotriphosphazene
- Cylindrical microelectrodes
- Cymantrene
- CYP11A1
- CYP1A2
- CYP2B4
- CYP3A6
- CYP450
- Cysteine
- Cysteine peptides
- Cytochrome c
- Cytochrome P-450
- Cytochrome P450
- Cytochrome P450 3A
- Cytochromes
- Cytochromes P-450
- Cytochromes P450
- Cytokinins
- Cytoprotective effect
- Cytosine
- Cytosine derivatives
- Cytosine modification
- Cytoskeleton
- Cytosolic reductases
- Cytostatic activity
- Cytostatic agents
- Cytostatics
- Cytotoxic agents
- Cytotoxic compounds
- Cytotoxic effect
- Cytotoxicity
- Cytotoxity of nucleosides
- Cytoxicity
- C–C coupling
