Jump to main content
Jump to site search

Issue 7, 2017
Previous Article Next Article

Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles

Author affiliations

Abstract

An efficient organoiodine-promoted intramolecular direct oxidative C(sp2)–N cross-coupling reaction was developed for the preparation of cyclopropyl spirooxindoles from readily available secondary cyclopropyl carboxamides.

Graphical abstract: Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles

Back to tab navigation

Supplementary files

Publication details

The article was received on 27 Feb 2017, accepted on 17 Apr 2017 and first published on 18 Apr 2017


Article type: Research Article
DOI: 10.1039/C7QO00156H
Citation: Org. Chem. Front., 2017,4, 1372-1375
  •   Request permissions

    Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles

    Z. Zhang, Y. Zhang, G. Huang and G. Zhang, Org. Chem. Front., 2017, 4, 1372
    DOI: 10.1039/C7QO00156H

Search articles by author

Spotlight

Advertisements