Chiral ammonium hypoiodite salt-catalyzed enantioselective oxidative cycloetherification to 2-acyl tetrahydrofurans

Muhammet Uyanik, Hiroki Hayashi, Hirokazu Iwata, Kazuaki Ishihara

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

2-Acyl tetrahydrofuran is a fundamental structure in natural products and pharmaceuticals. We achieved chiral quaternary ammonium hypoiodite salt-catalyzed enantioselective oxidative cycloetherification of δ-hydroxyketone derivatives. The corresponding 2-acyl tetrahydrofurans were obtained in high chemical yield with high enantioselectivity.

Original languageEnglish
Pages (from-to)353-355
Number of pages3
JournalChemistry Letters
Volume45
Issue number3
DOIs
Publication statusPublished - Jan 1 2016
Externally publishedYes

Fingerprint

Furans
Enantioselectivity
Biological Products
Ammonium Compounds
Salts
Derivatives
Pharmaceutical Preparations
tetrahydrofuran
hypoiodous acid

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Chiral ammonium hypoiodite salt-catalyzed enantioselective oxidative cycloetherification to 2-acyl tetrahydrofurans. / Uyanik, Muhammet; Hayashi, Hiroki; Iwata, Hirokazu; Ishihara, Kazuaki.

In: Chemistry Letters, Vol. 45, No. 3, 01.01.2016, p. 353-355.

Research output: Contribution to journalArticle

Uyanik, Muhammet ; Hayashi, Hiroki ; Iwata, Hirokazu ; Ishihara, Kazuaki. / Chiral ammonium hypoiodite salt-catalyzed enantioselective oxidative cycloetherification to 2-acyl tetrahydrofurans. In: Chemistry Letters. 2016 ; Vol. 45, No. 3. pp. 353-355.
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