Chemistry
(-)-Carvone
13%
4-Methoxyphenylacetic Acid
6%
Acetoxylation
6%
Acutumine
13%
Aflatoxin B2
13%
Alkane
8%
Alkene
8%
Alkylation
13%
Alkyne
13%
Androsterone
13%
Antiinfective
13%
Antitubercular
13%
Arylation
13%
Atropisomer
13%
Azaarene
13%
Bacterial Metabolite
13%
Base
13%
Benzaldehyde
48%
Benzocyclobutene
13%
Binding Site
13%
Biological Property
16%
Carbene
13%
Chemistry
37%
Cortistatin
13%
Crystal Structure
8%
Cyclic Structure
13%
Cyclohexene
13%
Cycloisomerization
13%
Cyclophane
13%
Cyclotrimerization
13%
Cytochrome P450
13%
Dehydrogenation
13%
Diazene
17%
Diels-Alder Reaction
46%
Dihydroxylation
13%
Edaxadiene
13%
Ene Reaction
26%
Epothilone A
26%
Epothilone B
13%
Fluorination
26%
Fumagillin
13%
Fumagillol
13%
Harziphilone
13%
Heterocyclic Compound
17%
Hispidospermidin
13%
Hydrogen
13%
Hydrogen Atom
8%
Hydroxyl
13%
Hydroxylation
13%
Immunosuppressive Agent
13%
Indane
13%
Intramolecular Michael Addition
13%
Keto Acids
13%
Ketone
13%
Lactone
11%
Luciferin
13%
Macrocycle
13%
Macrolide Antibiotic Agent
13%
Maraviroc
13%
Metabolite
13%
Metal Catalyst
8%
Methanesulfinic Acid
13%
Methyl Ester
13%
Methylation
13%
Mitragynine
13%
Molecular Scaffold
13%
Monoterpene
13%
Noble Metal
8%
Nucleophile
40%
Occurrence in Nature
100%
Octane
13%
Organic Chemistry
16%
Organic Compound
13%
Oxazolidinone
11%
Paclitaxel
26%
Peloruside A
13%
Pleuromutilin
13%
Polyketide
13%
Polymerization
13%
Potential Energy Barrier
6%
Reactive Intermediate
13%
Rhodium
13%
Ring Contraction
13%
Samarium
13%
Seebach Umpolung
13%
Sesquiterpenoid
13%
Shapiro Reaction
13%
Squalene
13%
Stannane
13%
Stereoisomer
13%
Stereoselective Synthesis
13%
Structure-Activity Relationship
13%
Suzuki Coupling
13%
Tautomer
13%
Transacetalization
13%
Transition State
15%
Triyne
13%
Tuberculostatic Agent
13%
Ugi Condensation
13%
Vancomycin
13%
Keyphrases
1,5-hydrogen Atom Transfer
13%
Abyssomicin
13%
Abyssomicin C
13%
Acceptorless Dehydrogenation
20%
Active Site Labeling
13%
Acutumine
13%
Acyl
13%
Alkanes
13%
Anti-infective
13%
Antibacterial Natural Products
13%
Antitubercular
13%
Aryl Ethers
13%
Aryl Iodides
13%
Base Metal Catalysis
13%
Benzaldehyde
13%
Bicyclization
13%
Biogenesis
13%
Biological Profile
13%
C-ring
13%
Carboxylesterase 1 (CES1)
13%
Chemical Profile
13%
Chemical Properties
13%
Chemical Strategies
13%
Chemical Synthesis
26%
Cobaloxime
13%
Concise Synthesis
26%
Construction Process
13%
Cortistatin
13%
CYP26A1
13%
CYP4Z1
13%
Dianion
13%
Double Annulation
13%
Earth-abundant
13%
Enantiospecific Synthesis
13%
Enzyme Class
13%
Epothilone B
13%
Epothilones
53%
Eschenmoser
26%
Fluorenone
13%
FR901483
13%
Fumagillin
13%
Functional Proteomics
13%
Functionalization Strategies
13%
Horner-Wadsworth-Emmons Reaction
13%
Hydrindanone
13%
Hypervalent Iodine
13%
In Vitro Reconstitution
13%
Intramolecular Michael Reaction
13%
Iodine-induced
13%
Jiadifenolide
13%
Knoevenagel Condensation
13%
Ligand Passivation
13%
Macrocyclization
26%
Maraviroc
13%
McMurry
13%
Mitsunobu Reaction
13%
Molecular Scaffold
13%
Multigrams
13%
Natural Product Synthesis
20%
Natural Products
13%
Nature-inspired
13%
New Antimicrobials
13%
New Ring System
13%
Novel Taxoids
13%
Organic Chemists
13%
Organic Compounds
13%
Organic Synthesis
13%
Oxya
20%
PA-824
13%
Particle-based
13%
Pd-catalyzed
13%
Pentacyclic
13%
Phosphate Ester
13%
Pleuromutilin
26%
Pleurotin
13%
Product Structure
20%
Reductive Acylation
13%
Retrosynthesis
13%
Rigid Framework
13%
Selective Elimination
13%
Sesquiterpenoids
13%
Shapiro Reaction
13%
Stereocontrolled
26%
Stereodivergent Synthesis
13%
Stereoselective Synthesis
13%
Structural Assignment
13%
Structural Reassignment
13%
Substrate Screening
13%
Sweet
13%
Synthetic Construction
13%
Target Discovery
13%
Taxol
13%
TNP-470
13%
Total Synthesis
26%
Transient Directing Group
13%
Tri-functional
13%
Uranyl Cation
13%
Vancomycin
13%
Verrucosispora
13%
Visible-light Photocatalyst
26%