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 *

320 related articles for article (PubMed ID: 16435838)

  • 1. Practical preparation method of polymer-incarcerated (PI) palladium catalysts using Pd(II) salts.
    Hagio H; Sugiura M; Kobayashi S
    Org Lett; 2006 Feb; 8(3):375-8. PubMed ID: 16435838
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel polymer incarcerated palladium with phosphinated polymers: active catalyst for Suzuki-Miyaura coupling without external phosphines.
    Nishio R; Sugiura M; Kobayashi S
    Org Lett; 2005 Oct; 7(22):4831-4. PubMed ID: 16235900
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The polymer incarcerated method for the preparation of highly active heterogeneous palladium catalysts.
    Akiyama R; Kobayashi S
    J Am Chem Soc; 2003 Mar; 125(12):3412-3. PubMed ID: 12643686
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mizoroki-Heck coupling using immobilized molecular precatalysts: leaching active species from Pd pincers, entrapped Pd salts, and Pd NHC complexes.
    Weck M; Jones CW
    Inorg Chem; 2007 Mar; 46(6):1865-75. PubMed ID: 17348717
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterogeneous versus homogeneous palladium catalysts for ligandless mizoroki-heck reactions: a comparison of batch/microwave and continuous-flow processing.
    Glasnov TN; Findenig S; Kappe CO
    Chemistry; 2009; 15(4):1001-10. PubMed ID: 19086042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Preparation of phosphinated polymer-incarcerated palladium and its application to C-N and C-C bond-forming reactions.
    Nishio R; Sugiura M; Kobayashi S
    Chem Asian J; 2007 Aug; 2(8):983-95. PubMed ID: 17591724
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Highly active palladium/activated carbon catalysts for Heck reactions: correlation of activity, catalyst properties, and Pd leaching.
    Köhler K; Heidenreich RG; Krauter JG; Pietsch J
    Chemistry; 2002 Feb; 8(3):622-31. PubMed ID: 11859857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mercaptopropyl-modified mesoporous silica: a remarkable support for the preparation of a reusable, heterogeneous palladium catalyst for coupling reactions.
    Crudden CM; Sateesh M; Lewis R
    J Am Chem Soc; 2005 Jul; 127(28):10045-50. PubMed ID: 16011367
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recoverable, reusable, highly active, and sulfur-tolerant polymer incarcerated palladium for hydrogenation.
    Okamoto K; Akiyama R; Kobayashi S
    J Org Chem; 2004 Apr; 69(8):2871-3. PubMed ID: 15074943
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genesis of coordinatively unsaturated palladium complexes dissolved from solid precursors during Heck coupling reactions and their role as catalytically active species.
    Köhler K; Kleist W; Pröckl SS
    Inorg Chem; 2007 Mar; 46(6):1876-83. PubMed ID: 17348718
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Suzuki-Miyaura coupling catalyzed by polymer-incarcerated palladium, a highly active, recoverable, and reusable Pd catalyst.
    Okamoto K; Akiyama R; Kobayashi S
    Org Lett; 2004 Jun; 6(12):1987-90. PubMed ID: 15176800
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Palladium nanoparticles captured in microporous polymers: a tailor-made catalyst for heterogeneous carbon cross-coupling reactions.
    Ogasawara S; Kato S
    J Am Chem Soc; 2010 Apr; 132(13):4608-13. PubMed ID: 20225817
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Aqueous-phase, palladium-catalyzed cross-coupling of aryl bromides under mild conditions, using water-soluble, sterically demanding alkylphosphines.
    DeVasher RB; Moore LR; Shaughnessy KH
    J Org Chem; 2004 Nov; 69(23):7919-27. PubMed ID: 15527271
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Self-assembled poly(imidazole-palladium): highly active, reusable catalyst at parts per million to parts per billion levels.
    Yamada YM; Sarkar SM; Uozumi Y
    J Am Chem Soc; 2012 Feb; 134(6):3190-8. PubMed ID: 22260520
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Suzuki-Miyaura coupling of aryl tosylates catalyzed by an array of indolyl phosphine-palladium catalysts.
    So CM; Lau CP; Chan AS; Kwong FY
    J Org Chem; 2008 Oct; 73(19):7731-4. PubMed ID: 18783275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dabco as an inexpensive and highly efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling reaction.
    Li JH; Liu WJ
    Org Lett; 2004 Aug; 6(16):2809-11. PubMed ID: 15281775
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tandem oxidative processes catalyzed by polymer-incarcerated multimetallic nanoclusters with molecular oxygen.
    Miyamura H; Kobayashi S
    Acc Chem Res; 2014 Apr; 47(4):1054-66. PubMed ID: 24661043
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.