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