Literature DB >> 15498017

Ferrocenyl monophosphine ligands: synthesis and applications in the Suzuki-Miyaura coupling of aryl chlorides.

Colin Baillie1, Lixin Zhang, Jianliang Xiao.   

Abstract

Ferrocenyl monophosphine ligands have been developed by a method based on palladium-catalyzed Suzuki-Miyaura coupling. The modular procedure creates a rapid synthesis of phosphines with diverse properties. The electron-rich phosphines have been successfully applied to the Suzuki-Miyaura coupling of activated and deactivated aryl chlorides, with low catalyst loading being feasible in the synthesis of tris-ortho-substituted biaryls.

Entities:  

Year:  2004        PMID: 15498017     DOI: 10.1021/jo048963u

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Nickel-catalyzed coupling of alkenes, aldehydes, and silyl triflates.

Authors:  Sze-Sze Ng; Chun-Yu Ho; Timothy F Jamison
Journal:  J Am Chem Soc       Date:  2006-09-06       Impact factor: 15.419

2.  Novel Phenothiazine-Bridged Porphyrin-(Hetero)aryl dyads: Synthesis, Optical Properties, In Vitro Cytotoxicity and Staining of Human Ovarian Tumor Cell Lines.

Authors:  Eva Molnar; Emese Gal; Luiza Gaina; Castelia Cristea; Eva Fischer-Fodor; Maria Perde-Schrepler; Patriciu Achimas-Cadariu; Monica Focsan; Luminita Silaghi-Dumitrescu
Journal:  Int J Mol Sci       Date:  2020-04-30       Impact factor: 5.923

  2 in total

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