Copper-Catalyzed Synthesis of 2-Unsubstituted, N-Substituted Benzimidazoles

Hirano K, Biju AT, Glorius F

Research article (journal)

Abstract

An efficient copper-catalyzed intramolecular arylation of formamidines forming 2-unsubstituted benzimidazoles in excellent yields is reported. Sixteen examples bearing sterically demanding substituents on nitrogen like Mes, 2,6-diisopropylphenyl, or 2-tert-butylphenyl and tolerating various functional groups demonstrate the utility of this method.

Details about the publication

JournalJournal of Organic Chemistry (J. Org. Chem.)
Volume74
Issue24
Page range9570-9572
StatusPublished
Release year2009 (18/12/2009)
Language in which the publication is writtenEnglish
DOI10.1021/jo902160y
Keywordsheterocyclic carbene ligands cross-coupling reactions gamma-butyrolactones conjugate umpolung azolium salts c-n 1,3-dimethylbenzimidazolium iodide alpha; beta-unsaturated aldehydes restricted flexibility palladium complexes

Authors from the University of Münster

Akkattu, Biju
Organic Chemistry Institute
Glorius, Frank
Professur für Organische Chemie (Prof. Glorius)