Chemistry
1,8-naphthyridine
13%
2-Naphthol
26%
3-Bromopyridine
26%
Acetal
17%
Acylimine
26%
Alkylation
33%
Allylic Alkylation
40%
Amino Acid
20%
Amino Alcohol
26%
Aprepitant
13%
Asymmetric Synthesis
100%
Aza-Diels-Alder Reaction
26%
Azetidin-2-One
13%
Base
20%
Benzaldehyde
13%
Carbapenem
66%
Carbene
20%
Carboxamide
31%
Catalyst Synthesis
13%
Chiral Reagent
13%
Cholecystokinin Receptor Blocking Agent
13%
Chromium Trioxide
13%
Condensation
40%
Coupling Reaction
26%
Cross-Coupling Reaction
33%
Cyclodehydration
40%
Cyclopentanone
13%
Decarboxylation
33%
Diastereoselectivity
37%
Dibromopyridine
20%
Diels-Alder Reaction
44%
Diester
40%
Diol
33%
Dioxygen
20%
Dithioacetal
33%
Efavirenz
13%
Enantiomer
80%
Enantioselective Catalyst
13%
Enantioselectivity
37%
Endothelin A Receptor Antagonist
13%
Endothelin Receptor Antagonist
13%
Enolates
20%
Enzymatic Hydrolysis
33%
Epoxidation
40%
Epoxide
53%
Glyceraldehyde
13%
Growth Hormone Secretagogue
40%
Halide
46%
Heteroatom
20%
HIV Protease Inhibitor
53%
Hydrogenation
66%
Ibogamine
26%
Indane
20%
Indene
26%
Indole
53%
Jacobsen Epoxidation
20%
Ketoester
20%
Ketone
26%
Ketones
66%
Lactam
17%
Maytansinoid
13%
Mechanistic Study
26%
Methicillin
26%
Methyl Ester
20%
Michael Addition
20%
Molybdenum
31%
Nitrile
13%
Nitro Compound
17%
Organic Chemistry
13%
Oxazolidin-2-One
13%
Oxazoline
53%
Oxidative Addition
26%
Palladium
46%
Phenol
20%
Phosphodiesterase IV Inhibitor
26%
Phosphonate
13%
Pictet-Spengler Synthesis
13%
Piperazine
26%
Piperidones
20%
Pneumocandin B0
13%
Primary Structure
33%
Purity
33%
Pyridine N-Oxide
16%
Racemate
20%
Regioselectivity
20%
Ring Formation
46%
Ritter Amidation
17%
Salen
20%
Serine
13%
Sharpless Asymmetric Aminohydroxylation
13%
Sharpless Asymmetric Dihydroxylation
26%
Silyl Enol Ether
13%
Stereochemistry
26%
Stereoselective Synthesis
86%
Styrene Oxide
26%
Substance P Antagonist
13%
Suzuki Coupling
13%
Thienamycin
13%
Transmetalation
13%
Trifluoromethylation
13%
Keyphrases
1,1′-binaphthyl
26%
1,8-naphthyridine
13%
2,4-disubstituted Quinolines
13%
2,4-pentanedione
13%
2-Arylpropionic Acids
13%
2-furaldehyde
13%
2-Naphthol
26%
2-Oxazolidinone
13%
3-amino-1
13%
4-pyridinecarboxaldehyde
13%
5-HT1D Receptor
26%
Acetalization Reaction
13%
Acylimines
26%
Air-stable Catalysts
13%
Amidation
13%
Amide Enolate
13%
Amino
13%
Aminoindan
20%
Anti-MRSA
26%
Anti-N
13%
Aprepitant
13%
Aryl
20%
Aryllithium Reagents
13%
Asymmetric Aminohydroxylation
13%
Asymmetric Hydroformylation
13%
Asymmetric Reduction
20%
Asymmetric Synthesis
53%
Azetidin-2-one
13%
Benzodiazepin
13%
Bicyclic Olefin
13%
Binaphthalene
26%
Boronic Acid Esters
13%
Carbapenem Antibiotics
13%
Carbenes
16%
Catalyst Synthesis
13%
Chloride
20%
Chromium Trioxide
13%
Conformationally Constrained
26%
Convergent Synthesis
20%
Coordinating Solvents
13%
COX-2 Inhibitors
26%
Crystallization-induced Diastereomer Transformation
13%
Cyclodehydration
26%
Diastereoselective Reaction
13%
Diester
26%
Diphenyl
13%
Dithioacetal
16%
Efficient Synthesis
26%
Enantioselective Catalyst
13%
Enzymatic Hydrolysis
20%
Esters
26%
Glycidyl
13%
Growth Hormone Secretagogue
40%
HIV Protease Inhibitors
33%
HMG-CoA Reductase Inhibitors
13%
Hydroxylated Metabolites
13%
Ibogamine
26%
Indole Synthesis
13%
Indole-2-carboxylic Acid
13%
Ketoesters
16%
Ketones
46%
Leukotriene B4 (LTB4)
26%
Maytansinoid
13%
Methyl
36%
Mibefradil
13%
Mitsunobu
26%
Mo(CO)6
13%
Mo-catalyzed
13%
N-tert-butanesulfinyl Imines
13%
Ni-catalyzed
13%
Nucleophilic
13%
Organic Chemistry
13%
Organozincates
26%
Overall Yield
33%
Oxazoline Ligands
13%
Pd-catalyzed Cross-coupling
26%
Phenylpiperidine
13%
Phosphine
26%
Phosphodiesterase-4 (PDE4)
26%
Phosphorus Pentoxide
13%
Pictet-Spengler Cyclization
13%
Pictet-Spengler Reaction
13%
Planar chiral
20%
Pneumocandin B0
13%
Practical Synthesis
44%
Preperation
13%
Prochiral
26%
Pyridine
33%
Rabbit Liver
13%
Racemate
26%
Sharpless Asymmetric Dihydroxylation
40%
Side Chain
20%
Stereoselective Synthesis
40%
Styrene Oxide
13%
Substance P
13%
Tert-butyl Ester
13%
Tetrahydronaphthyridine
13%
Thiazolium
26%
Thienamycin
13%
Trifluoromethylation
13%