Jump to main content
Jump to site search

Issue 12, 2007
Previous Article Next Article

First hypervalent iodine(III)-catalyzed C–N bond forming reaction: catalytic spirocyclization of amides to N-fused spirolactams

Author affiliations

Abstract

A protic solvent, 2,2,2-trifluoroethanol (CF3CH2OH), was successfully introduced into hypervalent iodine(III)-involved catalytic cycles as an effective solvent, and the first iodoarene-catalyzed intramolecular carbon–nitrogen bond forming reaction was achieved under strong acid-free and mild conditions.

Graphical abstract: First hypervalent iodine(iii)-catalyzed C–N bond forming reaction: catalytic spirocyclization of amides to N-fused spirolactams

Back to tab navigation
Please wait while Download options loads

Publication details

The article was received on 13 Nov 2006, accepted on 28 Nov 2006 and first published on 22 Dec 2006


Article type: Communication
DOI: 10.1039/B616510A
Citation: Chem. Commun., 2007, 1224-1226
  •   Request permissions

    First hypervalent iodine(III)-catalyzed C–N bond forming reaction: catalytic spirocyclization of amides to N-fused spirolactams

    T. Dohi, A. Maruyama, Y. Minamitsuji, N. Takenaga and Y. Kita, Chem. Commun., 2007, 1224
    DOI: 10.1039/B616510A

Search articles by author