Chemistry
Ethylenediamine
100%
Asymmetric Synthesis
57%
Purity
52%
Hydroamination
47%
Amino Acid
42%
Aspartic Acid
42%
Nitro Compound
42%
Sulfonylation
28%
Chemoselectivity
28%
Photocatalysis
28%
Ketones
28%
Ketone
28%
Primary Amine
28%
Prodrug
28%
Reductive Amination
28%
Heterocyclic Compound
28%
Diastereomer
28%
Alkylation
28%
Derivatization
28%
Nitroarene
28%
Flavin
28%
Carbonyl Compound
28%
Nitroolefin
28%
Indazole
28%
Enantiomer
23%
Agrochemical
23%
Biocatalyst
23%
Photocatalytic
14%
Enantiopurity
14%
Nitroalkene
14%
Nitroalkane
14%
Allyl Alcohol
14%
2-Aminophenol
14%
Primary Structure
14%
Nitro Group
14%
Enantioselectivity
14%
reduction of nitro
14%
Nef Reaction
14%
Donor
9%
formation of quinolines
9%
Agrochemical
9%
Monoamine
5%
Fumaric Acid
5%
Meropenem
5%
Carbapenem
5%
Isothermal Titration Calorimetry
5%
% Inhibition
5%
2H-Indazole
5%
Imine
5%
2-Nitrobenzaldehyde
5%
Keyphrases
Nitroreductase
57%
Enantioselectivity
33%
Bacillus Tequilensis
28%
Dihydrobenzoxazinone
28%
Dihydroquinoxalinones
28%
Pyrazolidinones
28%
Zinc Binder
28%
Ketone Reduction
28%
Nitroaliphatic
28%
Pharmaceutical Synthesis
28%
Flavoenzyme
23%
Ketones
23%
Optically Active Alcohols
23%
Anthranils
23%
Photocatalysis
19%
Pyrazolidin-3-ones
19%
Precision Delivery
14%
N-Sulfonylation
14%
MBL Inhibitors
14%
Global Deprotection
14%
Flavin-dependent
14%
Chemoselectivity
14%
Ene-reductase
14%
Photoenzymatic Synthesis
14%
Nef Reaction
14%
Photocatalytic System
14%
Tailored Synthesis
14%
Nitro Group Reduction
11%
Biocatalysis
9%
Chemoselective Reduction
9%
Synergistic Interaction
9%
Intramolecular Amidation
9%
Alcohol
9%
Enantiopurity
9%
Unsaturated Ketones
9%
Enantioselective Reduction
9%
Oxidoreductase
9%
High Conversion
9%
Acid-catalyzed Cyclization
9%
Non-native
9%
Allylic Alcohols
9%
Reaction Types
9%
N-heterocyclic Compounds
9%
Photobiocatalysis
9%
Carbonyl
9%
Nitro Compounds
9%
Ablation Resistance
7%
Nitropyrazoles
5%
2H-indazoles
5%
2-nitrobenzaldehyde
5%
Pharmacology, Toxicology and Pharmaceutical Science
Nitroreductase
57%
Ethylenediamine
42%
Aromatic Amine
35%
Penicillinase
34%
Riboflavin Derivative
34%
Metallo Beta Lactamase
28%
Bacilli
28%
Heterocyclic Compound
28%
Lyase
20%
Prodrug
14%
Infection
14%
Activated Carbon
9%
Malignant Neoplasm
7%
Azobenzene
7%
Prokaryote
7%
Aliphatic Amine
7%
Reducing Agent
7%
Nitro Derivative
7%
Eukaryote
7%
Antimicrobial Resistance
7%
Monoamine
5%
Calorimetry
5%
Carbapenem
5%
Fumaric Acid
5%
Escherichia coli
5%
Meropenem
5%
Nitrobenzene
5%
Sonidegib
5%
Sildenafil
5%
Pyrazole Derivative
5%
Linezolid
5%
Vismodegib
5%
Drug
5%
Pyridine Derivative
5%