Literature DB >> 14618571

Novel substrates for palladium-catalyzed coupling reactions of arenes.

Alexander Zapf1.   

Abstract

Arenes and heteroarenes are ubiquitous substructures in biologically active agents and new materials. Thus, functionalization ("refinement") of simple arene precursors is still of major importance for preparative organic chemistry. During the last 20 years, especially transition-metal-catalyzed cross-coupling reactions of aryl halides and triflates have given arene chemistry new impetus. The first industrial applications were realized a few years ago. Quite recently, carbonic acid derivatives such as anhydrides and esters have added to the scope of substrates for these coupling reactions. Some recent developments in this area are presented in this Minireview.

Entities:  

Year:  2003        PMID: 14618571     DOI: 10.1002/anie.200301681

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Highly-chemoselective step-down reduction of carboxylic acids to aromatic hydrocarbons via palladium catalysis.

Authors:  Chengwei Liu; Zhi-Xin Qin; Chong-Lei Ji; Xin Hong; Michal Szostak
Journal:  Chem Sci       Date:  2019-04-29       Impact factor: 9.825

  1 in total

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