Investigating N-methoxy-N'-aryl ureas in oxidative C-H olefination reactions: an unexpected oxidation behaviour.

Willwacher J, Rakshit S, Glorius F

Research article (journal) | Peer reviewed

Abstract

Herein, we report a urea derived directing group for mild and highly selective oxidative C-H bond olefination. Subsequent intramolecular Michael addition affords dihydroquinazolinones in good yields. The N-O bond of the urea substrate exhibits superior oxidative behaviour compared to a variety of other external oxidants.

Details about the publication

JournalOrganic and Biomolecular Chemistry (Org Biomol Chem)
Volume9
Issue13
Page range4736-4740
StatusPublished
Release year2011 (07/07/2011)
Language in which the publication is writtenUncoded languages
DOI10.1039/c1ob05636k

Authors from the University of Münster

Glorius, Frank
Professur für Organische Chemie (Prof. Glorius)