Rh Catalyzed Olefination and Vinylation of Unactivated Acetanilides

Patureau FW, Glorius F

Research article (journal)

Abstract

In the catalyzed oxidative olefination of acetanilides (oxidative-Heck coupling), Rh offers great advantages over more common Pd catalysts. Lower catalyst loadings, large functional group tolerance (in particular to halides), and higher reactivity of electron-neutral olefins (styrenes) are some of the attractive features. Most interestingly, even ethylene reacts to yield the corresponding acetanilido-styrene. Moreover, the Cu-II oxidant can also be utilized in catalytic amounts with air serving as the terminal oxidant.

Details about the publication

JournalJournal of the American Chemical Society (J. Am. Chem. Soc.)
Volume132
Issue29
Page range9982-9983
StatusPublished
Release year2010 (28/07/2010)
Language in which the publication is writtenEnglish
DOI10.1021/ja103834b
Keywordsh bond activation c-h aromatic substitution pd(ii)-catalyzed olefination direct arylation benzoic-acids functionalization indoles alkynes alkenylation

Authors from the University of Münster

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