Keyphrases
3D Structure
43%
Aglycon
40%
Aminals
40%
Base-labile
40%
Binding Site
40%
Biological Activity
40%
Carbamoyl
40%
Cascade Reaction
46%
Catalyst-free
60%
Click Chemistry
53%
Combinatorial Chemistry
40%
Computational Evolution
40%
Cyclic Peptide
80%
Cyclization
41%
Cysteine
40%
Cysteine Residues
40%
Diversity-oriented Synthesis
40%
Flow Synthesis
40%
Fluorobenzene
80%
Helicity
40%
Helix
55%
Hydrogen Bonds (H-bonds)
46%
Identifying Targets
40%
Imidazolone
40%
Imino
40%
Largazole
40%
Mannitol
40%
Mediated Synthesis
40%
Melanocortin 4 Receptor (MC4R)
40%
New Reactions
53%
Oral Absorption
40%
Organic Chemistry
40%
Peptide-based
40%
Pictet-Spengler Reaction
50%
Protecting Groups
40%
Protein Modification
40%
Proton-coupled Oligopeptide Transporter
40%
SNAr
80%
Solid Phase
83%
Solid Support
66%
Stereoselectivity
53%
Structure Motifs
40%
Sustainable Flow
40%
Tetrahydro-β-carboline
53%
Tetrahydroisoquinoline
53%
Thiazole
80%
Thiazoline
40%
YjdL
40%
β-glucosidase
40%
β-hairpin
40%
Chemistry
Acid Catalysis
40%
Acidic Condition
50%
Alkaline Condition
27%
Ambient Reaction Temperature
40%
Aminal
40%
Amino Acid
100%
Amino Aldehyde
20%
Aqueous Solution
20%
Arylation
20%
Base
40%
Benzamide
80%
Benzoic Acid
20%
Carbamoyl
40%
Cascade Reaction
20%
Chemistry
60%
Combinatorial Chemistry
40%
Cyclic Peptide
40%
Cyclic Structure
26%
Cysteine
40%
Drug Screening
20%
Enantioselectivity
20%
Fluorescence Resonance Energy Transfer
40%
Fluorobenzene
40%
formation
50%
Free Energy
40%
Hydrogen Bonding
20%
Indole
50%
Lactam
30%
Lewis Acid
40%
Macrocycle
40%
Molecular Model
40%
Neutral Condition
40%
Normal Mode
40%
Nucleophile
60%
Organic Acid
20%
Pentafluorobenzenes
40%
Pentapeptide
40%
Pictet-Spengler Synthesis
80%
Pool
20%
Protecting Group
40%
Protein-Protein Interaction
40%
proteolytic
40%
Pyrrole
40%
Reverse Turn
40%
stability
50%
Stereoselectivity
50%
Tetrapeptide
40%
Thiazole
40%
X-Ray Diffraction
40%
yellow
30%
