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 *

109 related articles for article (PubMed ID: 22685029)

  • 1. Higher-order zincates as transmetalators in alkyl-alkyl negishi cross-coupling.
    McCann LC; Hunter HN; Clyburne JA; Organ MG
    Angew Chem Int Ed Engl; 2012 Jul; 51(28):7024-7. PubMed ID: 22685029
    [TBL] [Abstract][Full Text] [Related]  

  • 2. On the remarkably different role of salt in the cross-coupling of arylzincs from that seen with alkylzincs.
    McCann LC; Organ MG
    Angew Chem Int Ed Engl; 2014 Apr; 53(17):4386-9. PubMed ID: 24677619
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Atroposelective Ni
    Groß D; van Otterlo WAL; Trapp O; Berthold D
    Chemistry; 2023 Dec; 29(67):e202302841. PubMed ID: 37665654
    [TBL] [Abstract][Full Text] [Related]  

  • 4. On the role of additives in alkyl-alkyl Negishi cross-couplings.
    Achonduh GT; Hadei N; Valente C; Avola S; O'Brien CJ; Organ MG
    Chem Commun (Camb); 2010 Jun; 46(23):4109-11. PubMed ID: 20520876
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst.
    Hadei N; Kantchev EA; O'Brien CJ; Organ MG
    J Org Chem; 2005 Oct; 70(21):8503-7. PubMed ID: 16209599
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aryl ether as a Negishi coupling partner: an approach for constructing C-C bonds under mild conditions.
    Wang C; Ozaki T; Takita R; Uchiyama M
    Chemistry; 2012 Mar; 18(12):3482-5. PubMed ID: 22374683
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).
    Terao J; Kambe N
    Acc Chem Res; 2008 Nov; 41(11):1545-54. PubMed ID: 18973349
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The first Negishi cross-coupling reaction of two alkyl centers utilizing a Pd-N-heterocyclic carbene (NHC) catalyst.
    Hadei N; Kantchev EA; O'Brien CJ; Organ MG
    Org Lett; 2005 Aug; 7(17):3805-7. PubMed ID: 16092880
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates.
    Zhou J; Fu GC
    J Am Chem Soc; 2003 Oct; 125(41):12527-30. PubMed ID: 14531697
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Role of LiBr and ZnBr
    Eckert P; Organ MG
    Chemistry; 2019 Dec; 25(69):15751-15754. PubMed ID: 31544269
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Density functional theory investigation of the alkyl-alkyl Negishi cross-coupling reaction catalyzed by N-heterocyclic carbene (NHC)-Pd complexes.
    Chass GA; O'Brien CJ; Hadei N; Kantchev EA; Mu WH; Fang DC; Hopkinson AC; Csizmadia IG; Organ MG
    Chemistry; 2009; 15(17):4281-8. PubMed ID: 19288489
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Salt to Taste: The Critical Roles Played by Inorganic Salts in Organozinc Formation and in the Negishi Reaction.
    Eckert P; Sharif S; Organ MG
    Angew Chem Int Ed Engl; 2021 May; 60(22):12224-12241. PubMed ID: 32986262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms.
    Phapale VB; Cárdenas DJ
    Chem Soc Rev; 2009 Jun; 38(6):1598-607. PubMed ID: 19587955
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Theoretical study on the mechanism of Ni-catalyzed alkyl-alkyl Suzuki cross-coupling.
    Li Z; Jiang YY; Fu Y
    Chemistry; 2012 Apr; 18(14):4345-57. PubMed ID: 22374716
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rh-catalyzed Negishi alkyl-aryl cross-coupling leading to alpha- or beta-phosphoryl-substituted alkylarenes.
    Takahashi H; Inagaki S; Yoshii N; Gao F; Nishihara Y; Takagi K
    J Org Chem; 2009 Apr; 74(7):2794-7. PubMed ID: 19267488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cobalt-catalyzed negishi cross-coupling reactions of (hetero)arylzinc reagents with primary and secondary alkyl bromides and iodides.
    Hammann JM; Haas D; Knochel P
    Angew Chem Int Ed Engl; 2015 Apr; 54(15):4478-81. PubMed ID: 25694155
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst.
    Organ MG; Avola S; Dubovyk I; Hadei N; Kantchev EA; O'Brien CJ; Valente C
    Chemistry; 2006 Jun; 12(18):4749-55. PubMed ID: 16568493
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cationic intermediates in the Pd-catalyzed negishi coupling. kinetic and density functional theory study of alternative transmetalation pathways in the Me-Me coupling of ZnMe2 and trans-[PdMeCl(PMePh2)2].
    García-Melchor M; Fuentes B; Lledós A; Casares JA; Ujaque G; Espinet P
    J Am Chem Soc; 2011 Aug; 133(34):13519-26. PubMed ID: 21793573
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides.
    Zhou JS; Fu GC
    J Am Chem Soc; 2003 Dec; 125(48):14726-7. PubMed ID: 14640646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The first iron-catalysed aluminium-variant Negishi coupling: critical effect of co-existing salts on the dynamic equilibrium of arylaluminium species and their reactivity.
    Kawamura S; Ishizuka K; Takaya H; Nakamura M
    Chem Commun (Camb); 2010 Sep; 46(33):6054-6. PubMed ID: 20657915
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.