These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 17389995)

  • 1. Nitrogen-doped magnetic carbon nanoparticles as catalyst supports for efficient recovery and recycling.
    Yoon H; Ko S; Jang J
    Chem Commun (Camb); 2007 Apr; (14):1468-70. PubMed ID: 17389995
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recycling of homogeneous Pd catalysts using superparamagnetic nanoparticles as novel soluble supports for Suzuki, Heck, and Sonogashira cross-coupling reactions.
    Stevens PD; Li G; Fan J; Yen M; Gao Y
    Chem Commun (Camb); 2005 Sep; (35):4435-7. PubMed ID: 16136242
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Immobilization of palladium in mesoporous silica matrix: preparation, characterization, and its catalytic efficacy in carbon-carbon coupling reactions.
    Jana S; Dutta B; Bera R; Koner S
    Inorg Chem; 2008 Jun; 47(12):5512-20. PubMed ID: 18459724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Palladium catalysts supported on mesoporous molecular sieves bearing nitrogen donor groups: preparation and use in Heck and Suzuki C-C bond-forming reactions.
    Demel J; Lamac M; Cejka J; Stepnicka P
    ChemSusChem; 2009; 2(5):442-51. PubMed ID: 19418499
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diatomite-supported Pd nanoparticles: an efficient catalyst for Heck and Suzuki reactions.
    Zhang Z; Wang Z
    J Org Chem; 2006 Sep; 71(19):7485-7. PubMed ID: 16958549
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pd on porous glass: a versatile and easily recyclable catalyst for Suzuki and Heck reactions.
    Schmöger C; Szuppa T; Tied A; Schneider F; Stolle A; Ondruschka B
    ChemSusChem; 2008; 1(4):339-47. PubMed ID: 18605100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Magnetically separable Pd catalyst for carbonylative Sonogashira coupling reactions for the synthesis of alpha,beta-alkynyl ketones.
    Liu J; Peng X; Sun W; Zhao Y; Xia C
    Org Lett; 2008 Sep; 10(18):3933-6. PubMed ID: 18722455
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Palladium nanoparticles supported on an organic-inorganic fluorinated hybrid material. Application to microwave-based heck reaction.
    Niembro S; Shafir A; Vallribera A; Alibés R
    Org Lett; 2008 Aug; 10(15):3215-8. PubMed ID: 18576660
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Palladium nanoparticles on graphite oxide and its functionalized graphene derivatives as highly active catalysts for the Suzuki-Miyaura coupling reaction.
    Scheuermann GM; Rumi L; Steurer P; Bannwarth W; Mülhaupt R
    J Am Chem Soc; 2009 Jun; 131(23):8262-70. PubMed ID: 19469566
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phosphine-free perfluoro-tagged palladium nanoparticles supported on fluorous silica gel: application to the Heck reaction.
    Bernini R; Cacchi S; Fabrizi G; Forte G; Niembro S; Petrucci F; Pleixats R; Prastaro A; Sebastián RM; Soler R; Tristany M; Vallribera A
    Org Lett; 2008 Feb; 10(4):561-4. PubMed ID: 18205367
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spatially controlled Suzuki and Heck catalytic molecular coupling.
    Davis JJ; Bagshaw CB; Busuttil KL; Hanyu Y; Coleman KS
    J Am Chem Soc; 2006 Nov; 128(43):14135-41. PubMed ID: 17061897
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions.
    Marion N; Nolan SP
    Acc Chem Res; 2008 Nov; 41(11):1440-9. PubMed ID: 18774825
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pd on surface-modified NiFe2O4 nanoparticles: a magnetically recoverable catalyst for Suzuki and Heck reactions.
    Baruwati B; Guin D; Manorama SV
    Org Lett; 2007 Dec; 9(26):5377-80. PubMed ID: 18020449
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ordered mesoporous Pd/silica-carbon as a highly active heterogeneous catalyst for coupling reaction of chlorobenzene in aqueous media.
    Wan Y; Wang H; Zhao Q; Klingstedt M; Terasaki O; Zhao D
    J Am Chem Soc; 2009 Apr; 131(12):4541-50. PubMed ID: 19275234
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Thermally reduced ruthenium nanoparticles as a highly active heterogeneous catalyst for hydrogenation of monoaromatics.
    Su F; Lv L; Lee FY; Liu T; Cooper AI; Zhao XS
    J Am Chem Soc; 2007 Nov; 129(46):14213-23. PubMed ID: 17973376
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of small palladium nanoparticles stabilized by bisphosphine BINAP bearing an alkyl chain and their palladium nanoparticle-catalyzed carbon-carbon coupling reactions under room-temperature.
    Tatumi R; Akita T; Fujihara H
    Chem Commun (Camb); 2006 Aug; (31):3349-51. PubMed ID: 16883433
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Triazine-based polymers as nanostructured supports for the liquid-phase oxidation of alcohols.
    Chan-Thaw CE; Villa A; Prati L; Thomas A
    Chemistry; 2011 Jan; 17(3):1052-7. PubMed ID: 21226123
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Palladium catalyzed Suzuki C-C couplings in an ionic liquid: nanoparticles responsible for the catalytic activity.
    Fernández F; Cordero B; Durand J; Muller G; Malbosc F; Kihn Y; Teuma E; Gómez M
    Dalton Trans; 2007 Dec; (47):5572-81. PubMed ID: 18043820
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Palladium nanoclusters supported on propylurea-modified siliceous mesocellular foam for coupling and hydrogenation reactions.
    Erathodiyil N; Ooi S; Seayad AM; Han Y; Lee SS; Ying JY
    Chemistry; 2008; 14(10):3118-25. PubMed ID: 18260070
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pd-catalyzed efficient one-pot sequential cross-coupling reactions of aryl dihalides.
    Zhang X; Liu A; Chen W
    Org Lett; 2008 Sep; 10(17):3849-52. PubMed ID: 18681450
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.