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 *

205 related articles for article (PubMed ID: 29292462)

  • 1. Miyaura borylation/Suzuki-Miyaura coupling (MBSC) sequence of 4-bromo-2,4'-bithiazoles with halides: straightforward access to a heterocylic cluster of d-series of thiopeptide GE2270.
    Lassalas P; Berini C; Rouchet JEY; Hédouin J; Marsais F; Schneider C; Baudequin C; Hoarau C
    Org Biomol Chem; 2018 Jan; 16(4):526-530. PubMed ID: 29292462
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis of 8-arylquinolines via one-pot Pd-catalyzed borylation of quinoline-8-yl halides and subsequent Suzuki-Miyaura coupling.
    Zhang Y; Gao J; Li W; Lee H; Lu BZ; Senanayake CH
    J Org Chem; 2011 Aug; 76(15):6394-400. PubMed ID: 21662971
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Highly efficient borylation Suzuki coupling process for 4-bromo-2-ketothiazoles: straightforward access to micrococcinate and saramycetate esters.
    Martin T; Laguerre C; Hoarau C; Marsais F
    Org Lett; 2009 Aug; 11(16):3690-3. PubMed ID: 19624105
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Palladium(0)-catalyzed suzuki-miyaura cross-coupling reactions of potassium aryl- and heteroaryltrifluoroborates with alkenyl bromides.
    Molander GA; Fumagalli T
    J Org Chem; 2006 Jul; 71(15):5743-7. PubMed ID: 16839157
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C-H Arylation/Ring-Transformation Strategy.
    Amaike K; Itami K; Yamaguchi J
    Chemistry; 2016 Mar; 22(13):4384-8. PubMed ID: 26833497
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Suzuki-Miyaura cross-coupling reactions of unprotected haloimidazoles.
    Tan J; Chen Y; Li H; Yasuda N
    J Org Chem; 2014 Sep; 79(18):8871-6. PubMed ID: 25140886
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A modular sydnone cycloaddition/Suzuki-Miyaura cross-coupling strategy to unsymmetrical 3,5-bis(hetero)aromatic pyrazoles.
    Delaunay T; Genix P; Es-Sayed M; Vors JP; Monteiro N; Balme G
    Org Lett; 2010 Aug; 12(15):3328-31. PubMed ID: 20597542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Palladium-catalyzed cross-coupling reaction of bis(pinacolato)diboron with 1-alkenyl halides or triflates: convenient synthesis of unsymmetrical 1,3-dienes via the borylation-coupling sequence.
    Takagi J; Takahashi K; Ishiyama T; Miyaura N
    J Am Chem Soc; 2002 Jul; 124(27):8001-6. PubMed ID: 12095344
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Concise and Atom-Economical Suzuki-Miyaura Coupling Reaction Using Unactivated Trialkyl- and Triarylboranes with Aryl Halides.
    Li H; Zhong YL; Chen CY; Ferraro AE; Wang D
    Org Lett; 2015 Jul; 17(14):3616-9. PubMed ID: 26125106
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly efficient monophosphine-based catalyst for the palladium-catalyzed suzuki-miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters.
    Billingsley K; Buchwald SL
    J Am Chem Soc; 2007 Mar; 129(11):3358-66. PubMed ID: 17326639
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Metalated aziridines for cross-coupling with aryl and alkenyl halides via palladium catalysis.
    Nelson JM; Vedejs E
    Org Lett; 2010 Nov; 12(22):5085-7. PubMed ID: 20945857
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid.
    Molander GA; Trice SL; Kennedy SM
    J Org Chem; 2012 Oct; 77(19):8678-88. PubMed ID: 22994557
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Catalyst-controlled regioselective Suzuki couplings at both positions of dihaloimidazoles, dihalooxazoles, and dihalothiazoles.
    Strotman NA; Chobanian HR; He J; Guo Y; Dormer PG; Jones CM; Steves JE
    J Org Chem; 2010 Mar; 75(5):1733-9. PubMed ID: 20141223
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A nonsymmetric pincer-catalyzed Suzuki-Miyaura arylation of benzyl halides and other nonactivated unusual coupling partners.
    Inés B; Moreno I; SanMartin R; Domínguez E
    J Org Chem; 2008 Nov; 73(21):8448-51. PubMed ID: 18855448
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of a Sulfur-Modified Glass-Supported Pd Nanoparticle Catalyst for Suzuki-Miyaura Coupling.
    Xiao M; Hoshiya N; Fujiki K; Honma T; Tamenori Y; Shuto S; Fujioka H; Arisawa M
    Chem Pharm Bull (Tokyo); 2016; 64(8):1154-60. PubMed ID: 27477655
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Palladium-catalyzed borylation of aryl (pseudo)halides and its applications in biaryl synthesis.
    Ji H; Cai J; Gan N; Wang Z; Wu L; Li G; Yi T
    Chem Cent J; 2018 Dec; 12(1):136. PubMed ID: 30564982
    [TBL] [Abstract][Full Text] [Related]  

  • 17. One-pot primary aminomethylation of aryl and heteroaryl halides with sodium phthalimidomethyltrifluoroborate.
    Murai N; Miyano M; Yonaga M; Tanaka K
    Org Lett; 2012 Jun; 14(11):2818-21. PubMed ID: 22591586
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Scope of aminomethylations via Suzuki-Miyaura cross-coupling of organotrifluoroborates.
    Molander GA; Gormisky PE; Sandrock DL
    J Org Chem; 2008 Mar; 73(6):2052-7. PubMed ID: 18284257
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Palladium-catalyzed cross-coupling between vinyl halides and tert-butyl carbazate: first general synthesis of the unusual N-Boc-N-alkenylhydrazines.
    Barluenga J; Moriel P; Aznar F; Valdés C
    Org Lett; 2007 Jan; 9(2):275-8. PubMed ID: 17217283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Palladium-catalyzed synthesis of 2,3,4-trisubstituted furans via cascade reactions of aryloxy-enynes with aryl halides.
    Li E; Cheng X; Wang C; Shao Y; Li Y
    J Org Chem; 2012 Sep; 77(17):7744-8. PubMed ID: 22889051
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.