Oxidative cyclizations of oximes using hypervalent iodine reagents

Research output: Contribution to journalReview article

4 Citations (Scopus)

Abstract

This account overviews oxidative cyclization reactions of aldoximes or ketoximes promoted by hypervalent iodine reagents. The oxidation of aldoximes by iodine(III) compounds generates nitrile oxides which can further react with appropriate substrates via intermolecular or intramolecular 1,3-dipolar cycloaddition reactions leading to a variety of nitrogen and oxygen heterocycles. Hypervalent iodine reagents can also react with ketoximes producing the corresponding heterocyclic products via intramolecular cyclization reactions. Recently, the oxidative cyclization reactions of aldoximes have been realized under catalytic conditions mediated by hypervalent iodine active species.

Original languageEnglish
Pages (from-to)99-116
Number of pages18
JournalArkivoc
Volume2017
Issue number1
DOIs
Publication statusPublished - 24 Mar 2017

Fingerprint

Oximes
Cyclization
Iodine
Nitriles
Cycloaddition
Oxides
Nitrogen
Oxygen
Oxidation
Substrates

Keywords

  • 1
  • 3-dipolar cycloaddition
  • Heterocyclization
  • Hypervalent iodine
  • Iodine catalysis

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Oxidative cyclizations of oximes using hypervalent iodine reagents. / Yoshimura, Akira; Zhdankin, Viktor V.

In: Arkivoc, Vol. 2017, No. 1, 24.03.2017, p. 99-116.

Research output: Contribution to journalReview article

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