Chemistry
Organocatalysis
100%
Michael Reaction
43%
Enantioselectivity
38%
Michael Addition
35%
Cascade Reaction
29%
Pyrrolidine
26%
Fluorescent Dye
26%
Ketones
25%
Sulfonamide
24%
Thiourea
23%
Addition Reaction
22%
Aldol Reaction
19%
Amino Acid
18%
Nitroolefin
16%
Organocatalyst
14%
Primary Amine
14%
Cinchona Alkaloid
13%
Occurrence in Nature
13%
Ring Formation
12%
Secondary Amine
12%
Amino Acid Derivative
11%
Boronic Acid
11%
One Pot Reaction
10%
Enone
10%
Biaryl
9%
Nitroalkane
9%
Friedel-Crafts Reaction
9%
Indole
9%
Asymmetric Synthesis
9%
Enamine
9%
Oxindole
8%
Photoredox
8%
Stereoselective Synthesis
8%
Pyrrole
8%
Metallocene
7%
Isatin
7%
Alkene
7%
Donor
7%
Diastereoselectivity
7%
N-Tris(hydroxymethyl)methyl-2-Aminoethanesulfonic Acid
7%
Meso Porosity
7%
Palladium
7%
Formylation
7%
Chemoselectivity
7%
Hydrogenation
7%
Carboxylic Acid
6%
Hydrogen Bonding
6%
Polyene
6%
Organic Reaction
6%
Silyl Ether
6%
Keyphrases
Organocatalytic
29%
Enantioselectivity
26%
Aldehydes
16%
Enantioselective Conjugate Addition
15%
Sulfonamides
14%
Enantioselective Michael Addition
13%
Ketones
12%
Prodrug
12%
Pyrrolidine
11%
Michael Addition Reaction
11%
Nitroolefins
10%
High Enantioselectivity
10%
Amino Acid Derivatives
10%
Organocatalyst
9%
Coumarin-based
9%
Good Yield
9%
Amino Acids
9%
Unsaturated Aldehyde
8%
Esterase
7%
Enals
7%
Suzuki Coupling
7%
Asymmetric Hydrogenation
7%
Fluorous
7%
Enones
7%
Organocatalysis
7%
Amine Thiourea
7%
Aromatics
6%
Michael Reaction
6%
Diphenylprolinol
6%
Bifunctional
6%
Conjugate Addition
6%
Tryptophan Derivatives
6%
Efficient Synthesis
6%
Enantioenriched
5%
Peptidomimetics
5%
Fluorescent Probe
5%
Stereoselectivity
5%
Opioid Peptides
5%
Small Molecules
5%
Mild Reaction Conditions
5%
Pharmacology, Toxicology and Pharmaceutical Science
Prodrug
24%
Coumarin
19%
Mouse
18%
Malignant Neoplasm
15%
Esterase
12%
Phosphodiesterase
9%
Anticarcinogen
8%
Histone Deacetylase
8%
Drug Development
7%
Peptidomimetic Agent
7%
Indoleamine 2,3 Dioxygenase
7%
Drug Discovery
6%
Ferrous Ion
5%
IC50
5%
Opiate Peptide
5%