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A Sulfonative rearrangement of N-aryl sulfamates to para-sulfonyl anilines
Yifei Zhou,
Alan M Jones
Pharmacy
Research output
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Working paper/Preprint
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Preprint
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Keyphrases
Sulfonate
100%
Aniline
100%
Teraryl
100%
Aryl Aldehydes
100%
Sulfonyl
100%
Reaction Conditions
66%
Betaine
66%
Hydroxyl
33%
Functional Groups
33%
Thermal Control
33%
Heteroatom
33%
Sulfonation
33%
One-pot Reaction
33%
High Conversion
33%
Counterion Effect
33%
Ability to Change
33%
Sulfamate
33%
Lone Pair
33%
Isotope Experiments
33%
Bioactive Scaffolds
33%
Kinetic Isotope
33%
Two-step Procedure
33%
Ortho-para
33%
Forcing Temperature
33%
Sulfa
33%
Para-selective
33%
Heterocyclic Scaffolds
33%
Chemistry
Sulfamate
100%
Sulfonate
100%
Betaine
66%
Hydroxyl
33%
formation
33%
Counterion
33%
Heterocyclic Compound
33%
Sulfate
33%
Heteroatom
33%
sulfonation
33%
Chemical Engineering
Betaine
100%
Functional Group
50%