Jump to main content
Jump to site search

Issue 30, 2018
Previous Article Next Article

The radical acylarylation of N-arylacrylamides with aliphatic aldehydes using the photolysis of hypervalent iodine(III) reagents

Author affiliations

Abstract

This article describes a variety of 3,3-disubstituted 2-oxindoles that bear carbonyl groups, which are efficiently obtained from a radical reaction between N-arylacrylamides and aliphatic aldehydes. The reaction is initiated by the photolysis of hypervalent iodine(III) reagents and proceeds smoothly under mild, metal-free conditions.

Graphical abstract: The radical acylarylation of N-arylacrylamides with aliphatic aldehydes using the photolysis of hypervalent iodine(iii) reagents

Back to tab navigation

Supplementary files

Publication details

The article was received on 15 Jun 2018, accepted on 13 Jul 2018 and first published on 14 Jul 2018


Article type: Communication
DOI: 10.1039/C8OB01420E
Citation: Org. Biomol. Chem., 2018,16, 5412-5415
  •   Request permissions

    The radical acylarylation of N-arylacrylamides with aliphatic aldehydes using the photolysis of hypervalent iodine(III) reagents

    R. Sakamoto, N. Hirama and K. Maruoka, Org. Biomol. Chem., 2018, 16, 5412
    DOI: 10.1039/C8OB01420E

Search articles by author

Spotlight

Advertisements