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 *

141 related articles for article (PubMed ID: 20462189)

  • 1. Development of binaphthyl-based chiral dienes for rhodium(I)-catalyzed asymmetric arylation of N,N-dimethylsulfamoyl-protected aldimines.
    Cao Z; Du H
    Org Lett; 2010 Jun; 12(11):2602-5. PubMed ID: 20462189
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A ligand-library approach to the highly efficient rhodium/phosphoramidite-catalyzed asymmetric arylation of N,N-dimethylsulfamoyl-protected aldimines.
    Jagt RB; Toullec PY; Geerdink D; de Vries JG; Feringa BL; Minnaard AJ
    Angew Chem Int Ed Engl; 2006 Apr; 45(17):2789-91. PubMed ID: 16555344
    [No Abstract]   [Full Text] [Related]  

  • 3. Highly Enantioselective Arylation of N,N-Dimethylsulfamoyl-Protected Aldimines Using Simple Sulfur-Olefin Ligands: Access to Solifenacin and (S)-(+)-Cryptostyline II.
    Jiang T; Chen WW; Xu MH
    Org Lett; 2017 Apr; 19(8):2138-2141. PubMed ID: 28388063
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Vicinal-diamine-based chiral chain dienes as ligands for rhodium(I)-catalyzed highly enantioselective conjugated additions.
    Wang Y; Hu X; Du H
    Org Lett; 2010 Dec; 12(23):5482-5. PubMed ID: 21038876
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enantioselective rh-catalyzed arylation of N-tosylarylimines with arylboronic acids.
    Duan HF; Jia YX; Wang LX; Zhou QL
    Org Lett; 2006 Jun; 8(12):2567-9. PubMed ID: 16737315
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Design and Synthesis of Chiral Diene Ligands for Rh
    Syu JF; Lin HY; Cheng YY; Tsai YC; Ting YC; Kuo TS; Janmanchi D; Wu PY; Henschke JP; Wu HL
    Chemistry; 2017 Oct; 23(58):14515-14522. PubMed ID: 28766821
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rh-catalyzed enantioselective conjugate addition of arylboronic acids with a dynamic library of chiral tropos phosphorus ligands.
    Monti C; Gennari C; Piarulli U
    Chemistry; 2007; 13(5):1547-58. PubMed ID: 17133634
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rhodium-Catalyzed Enantioselective Arylation of Aliphatic Imines.
    Kato N; Shirai T; Yamamoto Y
    Chemistry; 2016 Jun; 22(23):7739-42. PubMed ID: 27119262
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diastereoselective and enantioselective Rh(I)-catalyzed additions of arylboronic acids to N-tert-butanesulfinyl and N-diphenylphosphinoyl aldimines.
    Weix DJ; Shi Y; Ellman JA
    J Am Chem Soc; 2005 Feb; 127(4):1092-3. PubMed ID: 15669835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Asymmetric nitroallylation of arylboronic acids with nitroallyl acetates catalyzed by chiral rhodium complexes and its application in a concise total synthesis of optically pure (+)-gamma-lycorane.
    Dong L; Xu YJ; Cun LF; Cui X; Mi AQ; Jiang YZ; Gong LZ
    Org Lett; 2005 Sep; 7(19):4285-8. PubMed ID: 16146408
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enantioselective rhodium-catalyzed addition of arylboronic acids to aldehydes using chiral spiro monophosphite ligands.
    Duan HF; Xie JH; Shi WJ; Zhang Q; Zhou QL
    Org Lett; 2006 Mar; 8(7):1479-81. PubMed ID: 16562921
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Palladium-catalyzed asymmetric arylation, vinylation, and allenylation of tert-cyclobutanols via enantioselective C-C bond cleavage.
    Matsumura S; Maeda Y; Nishimura T; Uemura S
    J Am Chem Soc; 2003 Jul; 125(29):8862-9. PubMed ID: 12862483
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Catalytic enantioselective arylation of N-tosylarylimines with arylboronic acids using C2-symmetric cationic N-heterocyclic carbene Pd(2+) diaquo complexes.
    Ma GN; Zhang T; Shi M
    Org Lett; 2009 Feb; 11(4):875-8. PubMed ID: 19140723
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rhodium/phosphoramidite-catalyzed asymmetric arylation of aldehydes with arylboronic acids.
    Jagt RB; Toullec PY; de Vries JG; Feringa BL; Minnaard AJ
    Org Biomol Chem; 2006 Mar; 4(5):773-5. PubMed ID: 16493458
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Preparation of C2-symmetric bicyclo[2.2.2]octa-2,5-diene ligands and their use for rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids.
    Otomaru Y; Okamoto K; Shintani R; Hayashi T
    J Org Chem; 2005 Apr; 70(7):2503-8. PubMed ID: 15787536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. C2-symmetric bicyclo[2.2.2]octadienes as chiral ligands: their high performance in rhodium-catalyzed asymmetric arylation of N-tosylarylimines.
    Tokunaga N; Otomaru Y; Okamoto K; Ueyama K; Shintani R; Hayashi T
    J Am Chem Soc; 2004 Oct; 126(42):13584-5. PubMed ID: 15493893
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Me-bipam for enantioselective ruthenium(II)-catalyzed arylation of aldehydes with arylboronic acids.
    Yamamoto Y; Kurihara K; Miyaura N
    Angew Chem Int Ed Engl; 2009; 48(24):4414-6. PubMed ID: 19418506
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The concise synthesis of chiral tfb ligands and their application to the rhodium-catalyzed asymmetric arylation of aldehydes.
    Nishimura T; Kumamoto H; Nagaosa M; Hayashi T
    Chem Commun (Camb); 2009 Oct; (38):5713-5. PubMed ID: 19774245
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rhodium-catalyzed enantioselective 1,6-addition of arylboronic acids to enynamides: asymmetric synthesis of axially chiral allenylsilanes.
    Nishimura T; Makino H; Nagaosa M; Hayashi T
    J Am Chem Soc; 2010 Sep; 132(37):12865-7. PubMed ID: 20806919
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chiral norbornadienes as efficient ligands for the rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids to fumaric and maleic compounds.
    Shintani R; Ueyama K; Yamada I; Hayashi T
    Org Lett; 2004 Sep; 6(19):3425-7. PubMed ID: 15355068
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.