Literature DB >> 20140914

UC Pd: a new form of Pd/C for Sonogashira couplings.

Christophe Duplais1, Arnold J Forman, Benjamin A Baker, Bruce H Lipshutz.   

Abstract

Screening of different sources of Pd/C shows reagents of highly variable nanoparticle sizes and oxidation states of the metal. Typically, catalysts with higher surface area are viewed as likely to be the more reactive. In this paper a new form of Pd/C, "UC Pd" is described that is shown to contain larger nanoparticles yet it is the most reactive catalyst of those sold commercially for Sonogashira coupling reactions. UC Pd functions efficiently in the absence of a copper co-catalyst, under very mild and "green" conditions using inexpensive 95% EtOH at 50 degrees C. It is also the only form of Pd/C that can be recycled. In side-by-side reactions with several commercially available forms of Pd/C, none compete successfully with UC Pd under standardized conditions. Physical data obtained from extensive surface analysis using TEM, XRD, XPS, and CO-TPD measurements lead to an explanation behind the unique reactivity of this new recyclable form of Pd/C.

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Year:  2010        PMID: 20140914      PMCID: PMC3959799          DOI: 10.1002/chem.200902471

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  14 in total

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3.  Sonogashira coupling of aryl halides catalyzed by palladium on charcoal.

Authors:  Zoltán Novák; András Szabó; József Répási; András Kotschy
Journal:  J Org Chem       Date:  2003-04-18       Impact factor: 4.354

4.  Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts.

Authors:  Lunxiang Yin; Jürgen Liebscher
Journal:  Chem Rev       Date:  2007-01       Impact factor: 60.622

5.  Synthesis of N-(3-arylpropyl)amino acid derivatives by Sonogashira types of reaction in aqueous media.

Authors:  M P López-Deber; L Castedo; J R Granja
Journal:  Org Lett       Date:  2001-09-06       Impact factor: 6.005

6.  Copper-in-charcoal (Cu/C): heterogeneous, copper-catalyzed asymmetric hydrosilylations.

Authors:  Bruce H Lipshutz; Bryan A Frieman; Anthony E Tomaso
Journal:  Angew Chem Int Ed Engl       Date:  2006-02-13       Impact factor: 15.336

7.  Palladium-catalyzed intramolecular coupling between aryl iodides and allyl moieties via thermal and microwave-assisted conditions.

Authors:  Mark Lautens; Eiji Tayama; Christelle Herse
Journal:  J Am Chem Soc       Date:  2005-01-12       Impact factor: 15.419

8.  Highly active palladium/activated carbon catalysts for Heck reactions: correlation of activity, catalyst properties, and Pd leaching.

Authors:  Klaus Köhler; Roland G Heidenreich; Jürgen G E Krauter; Jörg Pietsch
Journal:  Chemistry       Date:  2002-02-02       Impact factor: 5.236

9.  Efficient copper-free Sonogashira coupling of aryl chlorides with palladium on charcoal.

Authors:  Anna Komáromi; Zoltán Novák
Journal:  Chem Commun (Camb)       Date:  2008-09-08       Impact factor: 6.222

10.  Ligand-, copper-, and amine-free sonogashira reaction of aryl iodides and bromides with terminal alkynes.

Authors:  Sameer Urgaonkar; John G Verkade
Journal:  J Org Chem       Date:  2004-08-20       Impact factor: 4.354

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  1 in total

1.  Sonogashira reaction of aryl and heteroaryl halides with terminal alkynes catalyzed by a highly efficient and recyclable nanosized MCM-41 anchored palladium bipyridyl complex.

Authors:  Bo-Nan Lin; Shao-Hsien Huang; Wei-Yi Wu; Chung-Yuan Mou; Fu-Yu Tsai
Journal:  Molecules       Date:  2010-12-10       Impact factor: 4.411

  1 in total

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