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Keyphrases
Hydroxylamine
100%
Acyl
100%
2,3-Sigmatropic Rearrangement
91%
Fungi
83%
Triterpenoids
83%
Hydroxamic Acid
73%
Aryl
70%
Pisolithus Tinctorius
66%
Alkaloids
58%
Methyl
58%
Aromatics
55%
Teraryl
55%
Maleimide
50%
Phenanthridine
50%
Novel Synthesis
50%
New Synthesis
50%
Resin Acids
50%
Ingold
50%
Prelog
50%
X-ray Analysis
43%
N-substituted
41%
Synthetic Applications
33%
Carbazole Alkaloids
33%
Nitrones
33%
Aryl-aryl Coupling
33%
Chiroptical Properties
33%
In(III)
33%
Enamines
33%
Electronic Circular Dichroism
33%
Indolyl
33%
Indole
33%
O-acylation
33%
Trifluoromethanesulfonate
33%
Excellent Yields
33%
Cyanide
33%
Thiazolium Salts
33%
Amines
27%
Chemical Correlation
25%
Nuclear Overhauser Effect
25%
Alcohol
25%
Oxindole
25%
Aziridine
25%
X-ray Crystallography
25%
Differential Spectroscopy
25%
Aryl Radicals
25%
Stereochemical Hypothesis
25%
Double Bond
25%
Amino
25%
Intramolecular Addition
25%
Quaternary Salts
22%
Chemistry
Hydroxylamine
100%
Hydroxamic Acid
73%
Base
58%
formation
57%
Indole
50%
Phenanthridine
50%
Heterocyclic Compound
41%
Nitrone
33%
Enamine
33%
Alkene
33%
Electronic Circular Dichroism
33%
O-acylation
33%
Electrophile
33%
Carbazole Alkaloid
33%
Chemistry
33%
Resin Acid
33%
X-Ray Crystallography
33%
Thiamine
33%
MNDO Calculation
30%
Aryl Group
25%
Optical Activity
25%
Oxindole
25%
Tryptamine
25%
Molecular Model
25%
Spectroscopy
25%
Hartree-Fock Calculation
25%
Benzimidazole
20%
N-Bromosuccinimide
20%
X-Ray Spectroscopy
18%
Tryprostatin B
16%
Substitution Reaction
16%
Cinchona Alkaloid
16%
3-Aza-Cope Rearrangement
16%
Algicide
16%
Carboxylic Acid
16%
Anhydride
16%
Cyclohexenone
16%
Double Bond
16%
Heteroatom
16%
Palladium
16%
Rhoeadine
16%
Conformational Isomer
16%
Nuclear Overhauser Effect Difference Spectroscopy
16%
Acetyl
16%
Physical Method
16%
Triterpenoid
16%
Photocyclization
16%
Deuterium
16%
Skatole
16%
Physostigmine
16%
