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 *

127 related articles for article (PubMed ID: 12556176)

  • 1. Direct synthesis of ferrocenylmethylphosphines from ferrocenylmethyl alcohols and their application as ligands for room temperature Pd(0)-catalyzed Suzuki cross-couplings of aryl bromides.
    Tang ZY; Lu Y; Hu QS
    Org Lett; 2003 Feb; 5(3):297-300. PubMed ID: 12556176
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterogeneous Pd/C-catalyzed ligand-free, room-temperature Suzuki-Miyaura coupling reactions in aqueous media.
    Maegawa T; Kitamura Y; Sako S; Udzu T; Sakurai A; Tanaka A; Kobayashi Y; Endo K; Bora U; Kurita T; Kozaki A; Monguchi Y; Sajiki H
    Chemistry; 2007; 13(20):5937-43. PubMed ID: 17444548
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New air-stable planar chiral ferrocenyl monophosphine ligands: Suzuki cross-coupling of aryl chlorides and bromides.
    Jensen JF; Johannsen M
    Org Lett; 2003 Aug; 5(17):3025-8. PubMed ID: 12916972
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Guanidine/Pd(OAc)2-catalyzed room temperature Suzuki cross-coupling reaction in aqueous media under aerobic conditions.
    Li S; Lin Y; Cao J; Zhang S
    J Org Chem; 2007 May; 72(11):4067-72. PubMed ID: 17465565
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Macromolecular effect: synthesis of a ferrocenylmethylphosphine-containing polymer as highly efficient ligands for room-temperature palladium(0)-catalyzed Suzuki cross-coupling reactions of aryl chlorides.
    Hu QS; Lu Y; Tang ZY; Yu HB
    J Am Chem Soc; 2003 Mar; 125(10):2856-7. PubMed ID: 12617635
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel class of tertiary phosphine ligands based on a phospha-adamantane framework and use in the Suzuki cross-coupling reactions of aryl halides under mild conditions.
    Adjabeng G; Brenstrum T; Wilson J; Frampton C; Robertson A; Hillhouse J; McNulty J; Capretta A
    Org Lett; 2003 Mar; 5(6):953-5. PubMed ID: 12633114
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rapid room temperature Buchwald-Hartwig and Suzuki-Miyaura couplings of heteroaromatic compounds employing low catalyst loadings.
    Navarro O; Marion N; Mei J; Nolan SP
    Chemistry; 2006 Jun; 12(19):5142-8. PubMed ID: 16628762
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Simple amine/Pd(OAc)(2)-catalyzed suzuki coupling reactions of aryl bromides under mild aerobic conditions.
    Tao B; Boykin DW
    J Org Chem; 2004 Jun; 69(13):4330-5. PubMed ID: 15202886
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Palladium-catalyzed borylation of phenyl bromides and application in one-pot Suzuki-Miyaura biphenyl synthesis.
    Broutin PE; Cerna I; Campaniello M; Leroux F; Colobert F
    Org Lett; 2004 Nov; 6(24):4419-22. PubMed ID: 15548040
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recyclable and reusable Pd(OAc)2/DABCO/PEG-400 system for Suzuki-Miyaura cross-coupling reaction.
    Li JH; Liu WJ; Xie YX
    J Org Chem; 2005 Jul; 70(14):5409-12. PubMed ID: 15989320
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Practical synthesis of new and highly efficient ligands for the Suzuki reaction of aryl chlorides.
    Zapf A; Jackstell R; Rataboul F; Riermeier T; Monsees A; Fuhrmann C; Shaikh N; Dingerdissen U; Beller M
    Chem Commun (Camb); 2004 Jan; (1):38-9. PubMed ID: 14737321
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hexacationic Dendriphos ligands in the Pd-catalyzed Suzuki-Miyaura cross-coupling reaction: scope and mechanistic studies.
    Snelders DJ; van Koten G; Klein Gebbink RJ
    J Am Chem Soc; 2009 Aug; 131(32):11407-16. PubMed ID: 19639941
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis and characterization of monodisperse oligofluorenes.
    Jo J; Chi C; Höger S; Wegner G; Yoon DY
    Chemistry; 2004 Jun; 10(11):2681-8. PubMed ID: 15195299
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Efficient route to 1,3-Di-N-imidazolylbenzene. A comparison of monodentate vs bidentate carbenes in Pd-catalyzed cross coupling.
    Vargas VC; Rubio RJ; Hollis TK; Salcido ME
    Org Lett; 2003 Dec; 5(25):4847-9. PubMed ID: 14653689
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Efficient aqueous-phase Heck and Suzuki couplings of aryl bromides using tri(4,6-dimethyl-3- sulfonatophenyl)phosphine trisodium salt (TXPTS).
    Moore LR; Shaughnessy KH
    Org Lett; 2004 Jan; 6(2):225-8. PubMed ID: 14723534
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Efficient catalyst for the Suzuki-Miyaura coupling of potassium aryl trifluoroborates with aryl chlorides.
    Barder TE; Buchwald SL
    Org Lett; 2004 Aug; 6(16):2649-52. PubMed ID: 15281735
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Highly active palladium catalysts supported by bulky proazaphosphatrane ligands for Stille cross-coupling: coupling of aryl and vinyl chlorides, room temperature coupling of aryl bromides, coupling of aryl triflates, and synthesis of sterically hindered biaryls.
    Su W; Urgaonkar S; McLaughlin PA; Verkade JG
    J Am Chem Soc; 2004 Dec; 126(50):16433-9. PubMed ID: 15600345
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.