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SYNFACTS

SYNLETT

SYNTHESIS :

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Key Word List

The following list contains suggested key words for use in SYNTHESIS and SYNLETT.
Of the five key words chosen by authors, three should be from this list. These three key words can be expanded by the authors with their own choice of additional words.
For example: hypervalent iodine, alkenes, enantioselective metallation

The key word will be indexed under the word selected from the list and additional words will appear as subheadings.

This list is selected from key words that occurred regularly in SYNTHESIS/SYNLETT over the last three years. The list will be updated to meet the growing needs of synthetic organic chemists.

Acetals
Acylations
Addition reactions
Aggregation
Alcohols
Aldehydes
Aldol reactions
Alkaloids
Alkanes
Alkenation
Alkene complexes
Alkenes
Alkyl halides
Alkylations
Alkyne complexes
Alkynes
Allenes
Allylations
Allyl complexes
Aluminum
Amides
Aminations
Amines
Amino acids
Amino alcohols
Amino aldehydes
Annulations
Annulenes
Antibiotics
Antifungal agents
Antisense agents
Antitumor agents
Antiviral agents
Arene complexes
Arenes
Arylations
Arynes
Asymmetric amplification
Asymmetric catalysis
Asymmetric synthesis
Atropisomerism
Autocatalysis
Azapeptides
Azasugars
Azides
Azo compounds

Barium
Benzylation
Betaines
Biaryls
Bicyclic compounds
Biomimetic synthesis
Bioorganic chemistry
Biosynthesis
Boron
Bromine

Calixarenes
Carbanions
Carbene complexes
Carbenes
Carbenoids
Carbocations
Carbocycles
Carbohydrates
Carbonyl complexes
Carbonylations
Carboxylic acids
Catalysis
Catenanes
Cations
Cavitands
Chelates
Chemoselectivity
Chiral auxiliaries
Chiral pool
Chiral resolution
Chirality
Chromium
Chromophores
Cleavage
Clusters
Combinatorial chemistry
Complexes
Condensation
Conjugation
Copper
Coupling
Cross-coupling
Crown compounds
Cryptands
Cuprates
Cyanines
Cyanohydrins
Cyclizations
Cycloadditions
Cyclodextrines
Cyclopentadienes
Cyclophanes
 
Dehydrogenations
Dendrimers
Deoxygenation
Desulfurizations
Diastereoselectivity
Diazo compounds
Diene complexes
Diels-Alder reactions
Dihydroxylations
Dimerizations
Diols
Dioxiranes
DNA
Domino reactions
Drugs
Electrocyclic reactions
Electron transfer
Electrophilic additions
Electrophilic aromatic
substitutions
Eliminations
Enantiomeric resolution
Ene reactions
Enols
Enones
Enynes
Enzymes
Epoxidations
Epoxides
Esterification
Esters
Ethers

Fluorine
Free radicals
Fullerenes
Furans
Fused-ring systems

Gas-phase reactions
Genomics
Glycolipids
Glycopeptides
Glycosidases
Glycosides
Glycosylations
Green-chemistry
Grignard reactions

Halides
Halogenation
Halogens
Heck reaction
Helical structures
Heterocycles
Heterogenous catalysis
High-throughput screening
HIV
Homogenous catalysis
Host-guest systems
Hydrazones
Hydrides
Hydroborations
Hydrocarbons
Hydroformylations
Hydrogenation
Hydrogen transfer
Hydrogenations
Hydrolyses
Hydrosilylations
Hydrostannations
Hyperconjugation

Imides
Imines
Indium
Indoles
Induction
Inhibitors
Insertions
Iodine
Ionic liquids
Iridium
Iron
Isomerizations

Ketones
Kinetic resolution

Lactams
Lactones
Lanthanides
Lewis acids
Ligands
Lipids
Lithiation
Lithium

Macrocycles
Magnesium
Manganese
Mannich bases
Medicinal chemistry
Metalations
Metallacycles
Metallocenes
Metathesis
Michael additions
Mitsunobu reaction
Molecular recognition
Molybdenum
Multicomponent reactions
 
Nanostructures
Natural products
Neighboring-group
effects
Nickel
Nitriles
Nitrogen
Nucleobases
Nucleophiles
Nucleophilic additions
Nucleophilic aromatic
substitutions
Nucleosides
Nucleotides
 
Olefination
Oligomerization
Oligonucleotides
Oligosaccharides
Organometallic reagents
Osmium
Oxidations
Oxygen
Oxygenations
Ozonolysis

Palladacycles
Palladium
Peptides
Pericyclic reactions
Peroxides
Phase-transfer catalysis
Phenols
Pheromones
Phosphates
Phosphorus
Phosphorylations
Photochemistry
Photooxidations
Piperidines
Polyanions
Polycations
Polycycles
Polymers
Porphyrins
Prostaglandins
Protecting groups
Proteins
Protonations
Pyridines
Pyrroles

Quinones
Quinolines

Radical reactions
Radicals
Rearrangements
Receptors
Reductions
Regioselectivity
Retro reactions
Rhodium
Ring closure
Ring contractions
Ring expansion
Ring opening
Ruthenium

Samarium
Scandium
Schiff bases
Selenium
Self-assembly
Silicon
Sodium
Solid-phase synthesis
Solvent effects
Spectroscopy
Sphingolipids
Spiro compounds
Stereoselective synthesis
Stereoselectivity
Steric hindrance
Steroids
Stille reaction
Substituent effects
Sulfates
Sulfonamides
Sulfones
Sulfoxides
Sulfur
Supported catalysis
Supramolecular chemistry

Tandem reactions
Tautomerism
Terpenoids
Thioacetals
Thiols
Tin
Titanium
Total synthesis
Transesterifications
Transition metals
Transition states
Tungsten

Umpolung

Vinylidene complexes
Vitamins

Wacker reactions
Wittig reactions

Ylides

Zeolites
Zinc

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was released on October 28th, 2008. This release features 51 new active pharmaceutical ingredients and updates to 16 syntheses.

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ACS Awards for
Bernd Giese and
Hisashi Yamamoto

We would like to congratulate two of our SYNLETT Editors: Hisashi Yamamoto, who is being awarded the ACS Award for Creative Work in Synthetic Organic Chemistry 2009 and Bernd Giese, who is the recipient of the James Flack Norris Award in Physical Organic Chemistry 2009. Both awards will be presented in March 2009 at the 237th ACS National Meeting in Salt Lake City.

Interview with
Sir Jack Baldwin, FRS

Recently,
Sir Jack Baldwin, FRS was interviewed for SYNFORM by Laurence

Harwood and a SYNLETT Special Issue has been published on the occasion of his 70th birthday.

ACS Award for
Dieter Enders

We would like to congratulate Dieter Enders, Editor-in-Chief of SYNTHESIS,

on being awarded the Arthur C. Cope Scholar Award. The award will presented at the 236th ACS National Meeting in Philadelphia this month.

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