Endo-selective asymmetric inverse electron-demand 1,3-dipolar cycloaddition reaction of nitrones

Tomoko Ashizawa, Natsuki Ohtsuki, Tomoyuki Miura, Makoto Ohya, Takaomi Shinozaki, Taketo Ikeno, Tohru Yamada

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

In the presence of a catalytic amount of the optically active cobalt(III) hexafluoroantimonate, the inverse electron-demand 1,3-dipolar cycloaddition reaction of dihydrofuran with nitrones bearing an electron-withdrawing group effectively proceeded to afford the corresponding adducts with excellent endo-selectivity.{A figure is presented}.

Original languageEnglish
Pages (from-to)1801-1810
Number of pages10
JournalHeterocycles
Volume68
Issue number9
DOIs
Publication statusPublished - 2006 Sep 1

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Endo-selective asymmetric inverse electron-demand 1,3-dipolar cycloaddition reaction of nitrones'. Together they form a unique fingerprint.

  • Cite this