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 *

126 related articles for article (PubMed ID: 21623426)

  • 1. A highly active and selective palladium pincer catalyst for the formation of α-aryl ketones via cross-coupling.
    Bugarin A; Connell BT
    Chem Commun (Camb); 2011 Jul; 47(25):7218-20. PubMed ID: 21623426
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Negishi cross-coupling reaction catalyzed by an aliphatic, phosphine based pincer complex of palladium. biaryl formation via cationic pincer-type Pd(IV) intermediates.
    Gerber R; Blacque O; Frech CM
    Dalton Trans; 2011 Sep; 40(35):8996-9003. PubMed ID: 21691648
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis and X-ray structure determination of highly active Pd(II), Pd(I), and Pd(0) complexes of di(tert-butyl)neopentylphosphine (DTBNpP) in the arylation of amines and ketones.
    Hill LL; Crowell JL; Tutwiler SL; Massie NL; Hines CC; Griffin ST; Rogers RD; Shaughnessy KH; Grasa GA; Johansson Seechurn CC; Li H; Colacot TJ; Chou J; Woltermann CJ
    J Org Chem; 2010 Oct; 75(19):6477-88. PubMed ID: 20806983
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of a highly efficient alkylated pincer thioimido-palladium(II) complex as the active catalyst in Negishi coupling.
    Liu J; Wang H; Zhang H; Wu X; Zhang H; Deng Y; Yang Z; Lei A
    Chemistry; 2009; 15(17):4437-45. PubMed ID: 19288479
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rationally designed pincer-type heck catalysts bearing aminophosphine substituents: Pd IV intermediates and palladium nanoparticles.
    Bolliger JL; Blacque O; Frech CM
    Chemistry; 2008; 14(26):7969-77. PubMed ID: 18618875
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pincer-type Heck catalysts and mechanisms based on Pd(IV) intermediates: a computational study.
    Blacque O; Frech CM
    Chemistry; 2010 Feb; 16(5):1521-31. PubMed ID: 20024984
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mono- and binuclear cyclometallated palladium(II) complexes containing bridging (N,O-) and terminal (N-) imidate ligands: air stable, thermally robust and recyclable catalysts for cross-coupling processes.
    Fairlamb IJ; Kapdi AR; Lee AF; Sánchez G; López G; Serrano JL; García L; Pérez J; Pérez E
    Dalton Trans; 2004 Dec; (23):3970-81. PubMed ID: 15558122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 9-fluorenylphosphines for the Pd-catalyzed sonogashira, suzuki, and Buchwald-Hartwig coupling reactions in organic solvents and water.
    Fleckenstein CA; Plenio H
    Chemistry; 2007; 13(9):2701-16. PubMed ID: 17200923
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Palladium-catalyzed formylation of aryl bromides: elucidation of the catalytic cycle of an industrially applied coupling reaction.
    Sergeev AG; Spannenberg A; Beller M
    J Am Chem Soc; 2008 Nov; 130(46):15549-63. PubMed ID: 18956867
    [TBL] [Abstract][Full Text] [Related]  

  • 11. (t-Bu)2PN=P(i-BuNCH2CH2)3N: new efficient ligand for palladium-catalyzed C-N couplings of aryl and heteroaryl bromides and chlorides and for vinyl bromides at room temperature.
    Reddy ChV; Kingston JV; Verkade JG
    J Org Chem; 2008 Apr; 73(8):3047-62. PubMed ID: 18370424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A general palladium-catalyzed amination of aryl halides with ammonia.
    Schulz T; Torborg C; Enthaler S; Schäffner B; Dumrath A; Spannenberg A; Neumann H; Börner A; Beller M
    Chemistry; 2009; 15(18):4528-33. PubMed ID: 19322847
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Highly productive CNN pincer ruthenium catalysts for the asymmetric reduction of alkyl aryl ketones.
    Baratta W; Chelucci G; Magnolia S; Siega K; Rigo P
    Chemistry; 2009; 15(3):726-32. PubMed ID: 19053092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A SeCSe-Pd(II) pincer complex as a highly efficient catalyst for allylation of aldehydes with allyltributyltin.
    Yao Q; Sheets M
    J Org Chem; 2006 Jul; 71(14):5384-7. PubMed ID: 16808533
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Pd(Cl)2{P(NC5H10)(C6H11)2}2]--a highly effective and extremely versatile palladium-based Negishi catalyst that efficiently and reliably operates at low catalyst loadings.
    Bolliger JL; Frech CM
    Chemistry; 2010 Sep; 16(36):11072-81. PubMed ID: 20715208
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Symmetrical and unsymmetrical pincer complexes with group 10 metals: synthesis via aryl C-H activation and some catalytic applications.
    Niu JL; Hao XQ; Gong JF; Song MP
    Dalton Trans; 2011 May; 40(19):5135-50. PubMed ID: 21380463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Catalytic performance of symmetrical and unsymmetrical sulfur-containing pincer complexes: synthesis and tandem catalytic activity of the first PCS-pincer palladium complex.
    Gagliardo M; Selander N; Mehendale NC; van Koten G; Klein Gebbink RJ; Szabó KJ
    Chemistry; 2008; 14(16):4800-9. PubMed ID: 18432627
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Efficient Stille cross-coupling reaction using aryl chlorides or bromides in water.
    Wolf C; Lerebours R
    J Org Chem; 2003 Sep; 68(19):7551-4. PubMed ID: 12968920
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A highly efficient catalytic system for cross-coupling of aryl chlorides and bromides with malononitrile anion by palladium carbene complexes.
    Gao C; Tao X; Qian Y; Huang J
    Chem Commun (Camb); 2003 Jun; (12):1444-5. PubMed ID: 12841283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Catalytic efficiency of a new tridentate ferrocenyl phosphine auxiliary: Sonogashira cross-coupling reactions of alkynes with aryl bromides and chlorides at low catalyst loadings of 10(-1) to 10(-4) mol %.
    Hierso JC; Fihri A; Amardeil R; Meunier P; Doucet H; Santelli M; Ivanov VV
    Org Lett; 2004 Sep; 6(20):3473-6. PubMed ID: 15387526
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.