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An iodine(iii) mediated oxidative rearrangement of enamines: efficient synthesis of α-amino ketones
Published in Royal Society of Chemistry
2015
Volume: 51
   
Issue: 75
Pages: 14203 - 14206
Abstract
An iodine(iii)-mediated, group-selective oxidative rearrangement of β,β-diarylenamines to α-amino ketones has been accomplished with excellent yield. The developed reaction involves the initial oxidation of enamine to an α-acyloxyimine intermediate and concomitant semipinacol rearrangement. © The Royal Society of Chemistry.
About the journal
JournalData powered by TypesetChemical Communications
PublisherData powered by TypesetRoyal Society of Chemistry
ISSN13597345
Open AccessNo
Concepts (21)
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    DIPHENYLIODONIUM SALT
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    Enamine
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    Iodine
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    Ketone
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    Ketone derivative
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    Scavenger
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    TRIFLUOROACETIC ANHYDRIDE
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    Article
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    Chemical analysis
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    Chemical reaction
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    Chemical structure
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    Competition
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    Decomposition
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    Electron
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    Electrophilicity
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    Oxidation
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    OXIDATIVE REARRANGEMENT
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    Reaction optimization
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    Reaction time
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    Room temperature
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    Synthesis