- ISSN 0010-0765 printed
- ISSN 1212-6950 electronic
Keyword index
- Ab initio
- Ab initio calculation
- Ab initio calculations
- Ab initio CCSD(T) calculations
- Ab initio coupled Hartree-Fock
- Ab initio methods
- Ab initio molecular dynamics
- Ab initio nonempirical calculations
- Ab initio pair potential
- ab initio/IGLO calculations
- Ab initiocalculations
- Amathia convoluta
- ansa-Metallocenes
- ansa-Titanocene
- ansa-Zirconocene
- Arabidopsis thaliana
- Aronia melanocarpa
- Aspergillus oryzae
- Aspergillus tamarii
- Aspergillus terreus
- Aspergillus wentii
- A.c. oscillopolarography
- A25822 B
- A1AR functional studies
- AAS
- Ab inition calculations
- Abacavir 5'-phosphate
- Abnormal salt effect
- Abrasive stripping voltammetry
- Absolute configuration
- Absolute configuration assignment
- Absorption
- Absorption spectroscopy
- Acaricidal activity
- Accelerated heavy ions
- Acceleration of rate constant
- Acceptor compounds
- Accuracy
- Acenaphthene
- Acetal
- Acetals
- Acetic acid
- Acetic acid pulping
- Acetone
- Acetonitrile
- Acetophenone
- Acetophenones
- Acetosolv delignification
- Acetosolv process
- Acetyl groups
- Acetylacetonato complex
- Acetylation
- Acetylcholinesterase
- Acetylenedicarboxylate
- Acetylenes
- Acetylides
- Acetylpyrazine
- Acetylsalicylic acid
- Acid anhydrides
- Acid catalysis
- Acid hydrolysis
- Acid sites characterization
- Acid-base reactions
- Acid-catalysed addition reactions
- Acid-catalyzed decomposition
- Acidity
- Acidity constant
- Acidity constants
- Acidity function
- Acidity function construction
- Acidity functions
- Acidity strength
- Acido-basic reactions
- Acidobasic indicators
- Acridines
- Acrylates
- Activated carbon
- Activating and inhibitory receptors
- Activation
- Activation and detoxification
- Activation parameters
- Activators
- Active carbon
- Active carbon black Chezacarb
- Active esters
- Active sites
- Active sodium carbonate
- Activity coefficients
- Acyclic analogs
- Acyclic analogues
- Acyclic nucleoside analogues
- Acyclic nucleoside and nucleotide analogs
- Acyclic nucleoside and nucleotide analogues
- Acyclic nucleoside phophonates
- Acyclic nucleoside phosphonates
- Acyclic nucleosides
- Acyclic nucleotide analogs
- Acyclic nucleotide analogues
- Acyclovir
- Acyl chlorides
- Acyl transfer
- Acylal
- Acylation
- Acylations
- Acylselenoureas
- Adamantane
- Adaptor proteins
- Addition
- Addition of halo compounds
- Additions
- Adefovir
- Adenine
- Adenine derivatives
- Adenosine
- Adenosine deaminase
- Adenosine derivatives
- Adenosine phosphates
- Adenosine receptor antagonists
- Adenosine receptors
- Adenovirus
- Adenylate cyclase
- Adhesive interactions
- Adiabatic corrections
- Adiabatic electron affinity
- Adiabatic separation
- Adriamycin
- Adsorbed dithionate
- Adsorbed multilayers
- Adsorbed sulfur
- Adsorption
- Adsorption capacitance
- Adsorption effect
- Adsorption equilibrium
- Adsorption isotherm
- Adsorption isotherms
- Adsorption of CO2
- Adsorption of purine bases
- Adsorption on gold
- Adsorptive cathodic stripping voltammetry
- Adsorptive stripping voltammetry
- Adsorptivity
- AeCXE1 inhibitors
- Aerosol generator
- AES
- Affinity
- Affinity carrier ligand
- Affinity chromatography
- AFM
- AFM, AAS and FIB-SEM methods
- Ag-colloid
- Agarose
- Aggregated forms of proteins
- Aggregation
- Aggregation theory
- Agitation
- Agroclavine
- AIDS
- AISE
- AISE theory
- Ajugasterone C
- AK2
- Akermanite
- Al complexes
- Al-MCM-41
- AlCl3
- AlCl3·6H2O
- Alcohol synthesis
- Alcohols
- Alcohols effect
- Alcohols effects
- Alcoholysis
- Aldehyde
- Aldehydes
- Alditols
- Aldol condensation
- Aldol reaction
- Aldol reactions
- Alicyclic hydrocarbons
- Alignment of molecular axis
- Aliphatic compounds
- Alkali cations
- Alkali ions
- Alkali metal borides
- Alkali metal cations
- Alkali metal clusters
- Alkali metal ion selectivity
- Alkali metals
- Alkaline flooding
- Alkaline hydrolysis
- Alkaline water electrolysis
- Alkaloids
- Alkane disproportionation
- Alkanethiol monolayers
- Alkene complexes
- Alkene hydrogenation
- Alkene polymerization catalysts
- Alkenes
- Alkene–alkyne coupling
- Alkenylphosphonium salts
- Alkoxybenzoic acids
- Alkoxyboranes
- Alkoxycarbonylation
- Alkyl benzoates
- Alkyl coplexes
- Alkyl isocyanides
- Alkyl ligand
- Alkyl substituents
- Alkyl β-D-galactopyranoside
- Alkylammonium salts
- Alkylaromatics
- Alkylation
- Alkylation of benzene
- Alkylation of secondary amines
- Alkylations
- Alkylidene derivatives
- Alkyllithium reagents
- Alkyltin(IV) chlorides
- Alkyltin(IV) complexes
- Alkynals
- Alkyne
- Alkyne complexes
- Alkynes
- Alkynols
- Alkynylations
- Alkynylpurines
- Alkynylpyrimidine cyclizations
- Allenes
- Allocolchicine
- Allopregnanolone
- Allosteric binding
- Allosteric ligands
- Alloxazines
- Alloys
- Allyl complexes
- Allyl ethers
- Allyl-diene ligand
- Allylic oxidation
- Allylic rearrangement
- Allylic selenoxide
- Allylic substitution
- Allylic substitutions
- Allyllithium reagents
- Allyloxymethylmagnesium chloride
- AlPO-11
- AlPO-5
- AlPO4-n
- AlSBA-15
- Alternating current
- Alternating current voltammetry
- Alternative interpretation of substituent effects
- Alumina
- Aluminium
- Aluminium catalysts
- Aluminium triethoxide
- Aluminophosphate
- Aluminosilicate catalysts
- Aluminosilicates
- Aluminum
- Aluminum complexes
- AM1
- AM1 calculations
- AM1 method
- AM1/COSMO calculations
- Amalgams
- Amberlite XAD2 and XAD4
- Ambiguous base-pairing
- AMD473
- Amides
- Amides preparation
- Amidine
- Amidines
- Amidinium salts
- Amido-isodicyclopentadienyl ligand
- Amidolysis
- Amidoximes
- Amidrazone
- Aminations
- Amine
- Amine aggregation states
- Amine arylation
- Amine reductive alkylation
- Amine-functionalised carbaboranes
- Amineboranes
- Amines
- Amines reaction
- Amino acids
- Amino acids analogs
- Amino acids reaction
- Amino alcohols
- Amino aldehydes
- Amino sugars
- Amino-ortho-carboranethiolate
- Aminobenzoates
- Aminodiphenylamines
- Aminolysis
- Aminopeptidases
- Aminophosphines
- Aminophosphonate ligands
- Aminophosphonates
- Aminophosphonic acids
- Aminopropyl phosphonic acids
- Aminopyridines
- Aminosugars
- Aminothiatriazoles
- Amlodipine
- Ammine ligand decomposition
- Ammonia
- Ammonia synthesis
- Ammonium
- Ammonium acetate
- Ammonium formate
- Ammonium hypobromite
- Ammonium metavanadate as promotor
- Ammonium salts
- Amos-Musher theory
- Amostatine
- AMP
- AMP kinase
- Amperometric biosensor
- Amperometric detection
- Amperometric sensors
- Amperometry
- Amphiphiles
- Amphiphilic polymers
- Analgesic activity
- Analgesics
- Analytic derivatives
- Analytic model
- Analytic solution
- Analytic solutions
- Analytical applications
- Analytical methods
- Analytical solution
- ANC potentials
- Anchored catalysts
- Androstane
- Androstane derivatives
- Androstanes
- Anesthesia
- Angle resolved photoemission
- Anharmonic oscillations
- Anharmonic oscillator
- Anhydro derivatives
- Anhydro sugars
- Anhydronucleosides
- Anhydrosugars
- Anhydrous electrolytes
- Anhydrovinblastine
- Aniline
- Aniline derivatives
- Aniline oligomers
- Anilines
- Anion complexation
- Anion exchangers
- Anion hydration
- Anion receptors
- Anion recognition
- Anion-exchange
- Anionic micelles
- Anionic polymer resins
- Anionic polymerization
- Anions
- Anisotropic motion
- Annealed polyelectrolytes
- Annelation
- Annelation reactions
- Annulenes
- Anodic adsorptive stripping voltammetry
- Anodic electrochemically oxidized treatment time
- Anodic oxidation
- Anodic potential
- Anomerisation
- ANP
- Anpirtoline
- ANPs
- Antagonist
- Antagonists
- Anthocyanins
- Anthracenes
- Anthracenylthioureas
- Anthracyclins
- Anthranilanilides
- Anthranilates
- Anthraquinone
- Anti-aromatase activity
- Anti-HIV activity
- anti-Markovnikov rule
- Antiadiabatic state
- Antiandrogens
- Antiaromaticity
- Antiasthmatic effect
- Antiasthmatics
- Antibacterial activity
- Antibacterial and antifungal activity
- Antibacterial quinolones
- Antibiotics
- Antibodies
- Antibrassinolide activity
- Anticancer
- Anticancer activity
- Anticancer agents
- Anticancer drug
- Anticancer drugs
- Anticandidal agents
- Anticonvulsants
- Anticonvulsive effect
- Antidepressives
- Antiestrogenic activity
- Antiestrogens
- Antifeedant
- Antifeedant activity
- Antiferromagnetic
- Antifungal action
- Antifungal activity
- Antifungal agents
- Antifungals
- Antigens
- Antiglucocorticoid effect
- Antiglycation therapy
- Antihistaminics
- Antiinflammatory activity
- Antiinflammatory agents
- Antiinflammatory agents intermediates
- Antiinflammatory and antiasthmatic effects
- Antileukotrienic activities
- Antileukotrienic activity
- Antimetabolites
- Antimicrobial activity
- Antimitosis
- Antimony
- Antimycobacterial activity
- Antineoplastic
- Antineoplastic activity
- Antineoplastic agents
- Antineoplastics
- Antinociceptive activity
- Antioxidant activity
- Antioxidant properties
- Antioxidants
- Antiproliferative activity
- Antisense agents
- Antisense oligonucleotides
- Antithyroid drugs
- Antituberculotic activity
- Antituberculotics
- Antitumor activity
- Antitumor agents
- Antitumor drugs
- Antiviral activity
- Antiviral agents
- Antiviral drugs
- Antiviral evaluation
- Antiviral therapy
- Antivirals
- Aphidicolin
- Apoptotic and necrotic effects
- Apparent wall slip
- Applications
- Aprotic media
- Aprotic solvents
- Aptamers
- Aqueous chloroauric acid
- Aqueous conditions
- Aqueous droplets
- Aqueous solutions
- Araban
- Arbuzov reaction
- Arcyriarubine A
- Arene complexes
- Arenes
- Argon
- Aristolochic acids
- Aromatase inhibition
- Aromatase inhibitors
- Aromatic denitrocyclization
- Aromatic hydrocarbons
- Aromatic nucleophilic substitution
- Aromatic nucleophilic substitutions
- Aromaticity
- Aromatics
- Aromatization
- Aromatizations
- Array-based technologies
- Arsanes
- Arsenate sorption
- Arsenates
- Arsene fluoride
- Arsenic
- Arsenic(III)
- Arsenic(V)
- Arsines
- Artificial charge transfer
- Artificial chemistry
- Artificial life
- Artificial membranes
- Artificial neural network
- Aryl halides
- Aryl hydrazinecarboxylates
- Aryl-substituted resorc[4]arenes
- Arylacetic acids
- Arylacetylenes
- Arylboronic acids
- Arylmercuric halides
- Arynes
- As ligands
- Ascorbic acid
- Aspartic proteases
- Aspartic proteinase
- Aspartic proteinase inhibitors
- Aspidofractinine alkaloids
- Aspidophytine
- Aspidospermanes
- Aspirin
- Assignment of 13C NMR signals
- Assignment of signals
- Assisted ion transfer
- Association constants
- Association equilibrium
- Association rate
- Asteraceae
- Astrochemistry
- Asymmetric additions
- Asymmetric amplification
- Asymmetric autocatalysis
- Asymmetric catalysis
- Asymmetric conjugate additions
- Asymmetric hydroboration
- Asymmetric hydrogenation
- Asymmetric reductions
- Asymmetric synthesis
- Asymmetric tetraperoxodivanadate
- Asymptotic expansion
- Atmospheric chemistry
- Atom dipole interaction model
- Atom transfer
- Atom transfer radical polymerization
- Atom transfer radical polymerizations
- Atom-free radical
- Atomic absorption
- Atomic absorption spectroscopy
- Atomic and molecular energies
- Atomic emission spectrometry
- Atomic fluorine
- Atomic force microscopy
- Atomic iodine
- Atomic polarizabilities
- Atomic surfaces
- Atomization energies
- Atoms in molecules theory
- Atorvastatin
- ATP
- ATPases
- Atropisomerism
- Au catalysis
- Au clusters
- Au density calculation and measurement
- Au nanoparticles
- Au sputtering
- Au-Pt
- Au/NbOx interface
- Auger spectrum
- Autocatalysis
- Autocatalytic oxidation
- Autocatalytic reaction
- Autocorrelation function
- Autofluoresent nucleoside analogues
- Autohydrolysis
- Automated oligonucleotide synthesizer
- Automated solution handling
- Automorphism group of graph
- Autoxidation
- Autoxidative degradation
- Axial chirality
- Axial dispersion
- Axial impeller
- Axially chiral ligands
- Aza steroids
- Aza-crown macrocycles
- Azabicyclic
- Azaborane
- Azachalcones
- Azacrown
- Azacrown compounds
- Azacrown macrocycles
- Azacycle
- Azadecaboranes
- Azahelicenes
- Azametallaboranes
- Azanucleosides
- Azaphosphatranes
- Azasugars
- Azeotropic styrene-acrylonitrile copolymers
- Azepanes
- Azetidin-2-ones
- Azetidines
- Azides
- Azido compounds
- Azidohydroxylation
- Azidosugars
- Azines
- Aziridination
- Aziridines
- Azo compounds
- Azo coupling
- Azo coupling reaction
- Azo dyes
- Azobenzo[c]cinnoline
- Azoimide
- Azoles
- Azolopyridazines
- Azomethine
- Azomethine imides
- Azomethine ylides
- Azomethines
- Azoxy compounds
- AZT analogs
