Literature DB >> 17568471

FeCl3-catalyzed addition of 1,3-dicarbonyl compounds to aromatic olefins.

Jette Kischel1, Dirk Michalik, Alexander Zapf, Matthias Beller.   

Abstract

A direct, intermolecular addition of 1,3-dicarbonyl compounds to styrenes in the presence of FeCl3 as an inexpensive and disposable catalyst has been developed for the straightforward and practical synthesis of arylated diketones and ketoesters. The reactions proceed under mild conditions for most substrates (50-80 degrees C), and no strong acid or base is required. The synthetic value of the method is demonstrated by 15 examples, including the synthesis of the current pharmaceutical drug warfarin in one step and 42% yield from commercially available substrates.

Entities:  

Year:  2007        PMID: 17568471     DOI: 10.1002/asia.200700055

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  2 in total

1.  Bimetallic nanosized solids with acid and redox properties for catalytic activation of C-C and C-H bonds.

Authors:  Jose R Cabrero-Antonino; María Tejeda-Serrano; Manuel Quesada; Jose A Vidal-Moya; Antonio Leyva-Pérez; Avelino Corma
Journal:  Chem Sci       Date:  2016-08-26       Impact factor: 9.825

Review 2.  Methodologies for the synthesis of quaternary carbon centers via hydroalkylation of unactivated olefins: twenty years of advances.

Authors:  Thiago S Silva; Fernando Coelho
Journal:  Beilstein J Org Chem       Date:  2021-07-07       Impact factor: 2.883

  2 in total

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