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 *

179 related articles for article (PubMed ID: 25414056)

  • 1. Stereospecific couplings of secondary and tertiary boronic esters.
    Leonori D; Aggarwal VK
    Angew Chem Int Ed Engl; 2015 Jan; 54(4):1082-96. PubMed ID: 25414056
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development of Enantiospecific Coupling of Secondary and Tertiary Boronic Esters with Aromatic Compounds.
    Odachowski M; Bonet A; Essafi S; Conti-Ramsden P; Harvey JN; Leonori D; Aggarwal VK
    J Am Chem Soc; 2016 Aug; 138(30):9521-32. PubMed ID: 27384259
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Enantiospecific, regioselective cross-coupling reactions of secondary allylic boronic esters.
    Chausset-Boissarie L; Ghozati K; LaBine E; Chen JL; Aggarwal VK; Crudden CM
    Chemistry; 2013 Dec; 19(52):17698-701. PubMed ID: 24302640
    [No Abstract]   [Full Text] [Related]  

  • 4. Suzuki-Miyaura cross-couplings of secondary allylic boronic esters.
    Glasspoole BW; Ghozati K; Moir JW; Crudden CM
    Chem Commun (Camb); 2012 Jan; 48(9):1230-2. PubMed ID: 22179308
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enantiospecific sp(2)-sp(3) coupling of secondary and tertiary boronic esters.
    Bonet A; Odachowski M; Leonori D; Essafi S; Aggarwal VK
    Nat Chem; 2014 Jul; 6(7):584-9. PubMed ID: 24950327
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction.
    Molander GA; Ellis N
    Acc Chem Res; 2007 Apr; 40(4):275-86. PubMed ID: 17256882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Elucidating the Role of the Boronic Esters in the Suzuki-Miyaura Reaction: Structural, Kinetic, and Computational Investigations.
    Thomas AA; Zahrt AF; Delaney CP; Denmark SE
    J Am Chem Soc; 2018 Mar; 140(12):4401-4416. PubMed ID: 29543441
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transmetalation in the Suzuki-Miyaura coupling: the fork in the trail.
    Lennox AJ; Lloyd-Jones GC
    Angew Chem Int Ed Engl; 2013 Jul; 52(29):7362-70. PubMed ID: 23780626
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki-Miyaura Cross-Coupling of Boronic Esters.
    Delaney CP; Kassel VM; Denmark SE
    ACS Catal; 2020 Jan; 10(1):73-80. PubMed ID: 33585070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chemoselective Suzuki-Miyaura Cross-Coupling via Kinetic Transmetallation.
    Fyfe JW; Fazakerley NJ; Watson AJ
    Angew Chem Int Ed Engl; 2017 Jan; 56(5):1249-1253. PubMed ID: 27982480
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copper-catalyzed cross-coupling of boronic esters with aryl iodides and application to the carboboration of alkynes and allenes.
    Zhou Y; You W; Smith KB; Brown MK
    Angew Chem Int Ed Engl; 2014 Mar; 53(13):3475-9. PubMed ID: 24677502
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis of 3-(hetero)aryl tetrahydropyrazolo[3,4-c]pyridines by Suzuki-Miyaura cross-coupling methodology.
    Kemmitt PD; Blades K; Box MR; Dickinson S; Lamont GM; Madden K; McCoull W; Williams J
    J Org Chem; 2014 Aug; 79(16):7682-8. PubMed ID: 25050640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alkynyl Moiety for Triggering 1,2-Metallate Shifts: Enantiospecific sp
    Ganesh V; Odachowski M; Aggarwal VK
    Angew Chem Int Ed Engl; 2017 Aug; 56(33):9752-9756. PubMed ID: 28618129
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copper-mediated, palladium-catalyzed coupling of thiol esters with aliphatic organoboron reagents.
    Yu Y; Liebeskind LS
    J Org Chem; 2004 May; 69(10):3554-7. PubMed ID: 15132570
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hydrogen Atom Transfer Induced Boron Retaining Coupling of Organoboronic Esters and Organolithium Reagents.
    Wang D; Mück-Lichtenfeld C; Studer A
    J Am Chem Soc; 2019 Sep; 141(36):14126-14130. PubMed ID: 31454481
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Efficient catalysis of Suzuki-Miyaura C-C coupling reactions with palladium(II) complexes of partially hydrolyzed bisimine ligands: a process important in environment context.
    Kumar A; Rao GK; Saleem F; Kumar R; Singh AK
    J Hazard Mater; 2014 Mar; 269():9-17. PubMed ID: 24315812
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts.
    Han FS
    Chem Soc Rev; 2013 Jun; 42(12):5270-98. PubMed ID: 23460083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Simple palladium(II) precatalyst for Suzuki-Miyaura couplings: efficient reactions of benzylic, aryl, heteroaryl, and vinyl coupling partners.
    Burns MJ; Fairlamb IJ; Kapdi AR; Sehnal P; Taylor RJ
    Org Lett; 2007 Dec; 9(26):5397-400. PubMed ID: 18047357
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.