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 *

100 related articles for article (PubMed ID: 21302969)

  • 1. Design, synthesis, and evaluation of a helicenoidal DMAP Lewis base catalyst.
    Crittall MR; Rzepa HS; Carbery DR
    Org Lett; 2011 Mar; 13(5):1250-3. PubMed ID: 21302969
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The first magnetic nanoparticle-supported chiral DMAP analogue: highly enantioselective acylation and excellent recyclability.
    Gleeson O; Tekoriute R; Gun'ko YK; Connon SJ
    Chemistry; 2009 Jun; 15(23):5669-73. PubMed ID: 19388038
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Theoretical prediction of selectivity in kinetic resolution of secondary alcohols catalyzed by chiral DMAP derivatives.
    Larionov E; Mahesh M; Spivey AC; Wei Y; Zipse H
    J Am Chem Soc; 2012 Jun; 134(22):9390-9. PubMed ID: 22568686
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Design and synthesis of a new type of ferrocene-based planar chiral DMAP analogues. A new catalyst system for asymmetric nucleophilic catalysis.
    Seitzberg JG; Dissing C; Søtofte I; Norrby PO; Johannsen M
    J Org Chem; 2005 Oct; 70(21):8332-7. PubMed ID: 16209575
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Point-to-helical chirality transfer for a scalable and resolution-free synthesis of a helicenoidal DMAP organocatalyst.
    Crittall MR; Fairhurst NW; Carbery DR
    Chem Commun (Camb); 2012 Nov; 48(91):11181-3. PubMed ID: 22950085
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of enantiomerically pure C2-symmetric 4-pyrrolidinopyridine derivative as a chiral acyl transfer catalyst for the kinetic resolution of secondary alcohols.
    Naraku G; Shimomoto N; Hanamoto T; Inanaga J
    Enantiomer; 2000; 5(1):135-8. PubMed ID: 10763880
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A highly selective ferrocene-based planar chiral PIP (Fc-PIP) acyl transfer catalyst for the kinetic resolution of alcohols.
    Hu B; Meng M; Wang Z; Du W; Fossey JS; Hu X; Deng WP
    J Am Chem Soc; 2010 Dec; 132(47):17041-4. PubMed ID: 21058646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homobenzotetramisole: an effective catalyst for kinetic resolution of aryl-cycloalkanols.
    Birman VB; Li X
    Org Lett; 2008 Mar; 10(6):1115-8. PubMed ID: 18278928
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Asymmetric catalysis with "planar-chiral" derivatives of 4-(dimethylamino)pyridine.
    Fu GC
    Acc Chem Res; 2004 Aug; 37(8):542-7. PubMed ID: 15311953
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Oxidative kinetic resolution of racemic alcohols catalyzed by chiral ferrocenyloxazolinylphosphine-ruthenium complexes.
    Nishibayashi Y; Yamauchi A; Onodera G; Uemura S
    J Org Chem; 2003 Jul; 68(15):5875-80. PubMed ID: 12868920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structure-enantioselectivity effects in 3,4-dihydropyrimido[2,1-b]benzothiazole-based isothioureas as enantioselective acylation catalysts.
    Belmessieri D; Joannesse C; Woods PA; MacGregor C; Jones C; Campbell CD; Johnston CP; Duguet N; Concellón C; Bragg RA; Smith AD
    Org Biomol Chem; 2011 Jan; 9(2):559-70. PubMed ID: 21072411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Understanding the Reactivity and Selectivity of Fluxional Chiral DMAP-Catalyzed Kinetic Resolutions of Axially Chiral Biaryls.
    Maji R; Ugale H; Wheeler SE
    Chemistry; 2019 Mar; 25(17):4452-4459. PubMed ID: 30657217
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A trifunctional catalyst for one-pot synthesis of chiral diols via Heck coupling-N-oxidation-asymmetric dihydroxylation: application for the synthesis of diltiazem and taxol side chain.
    Choudary BM; Chowdari NS; Madhi S; Kantam ML
    J Org Chem; 2003 Mar; 68(5):1736-46. PubMed ID: 12608786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lewis base activation of Lewis acids. Vinylogous aldol reactions.
    Denmark SE; Beutner GL
    J Am Chem Soc; 2003 Jul; 125(26):7800-1. PubMed ID: 12822988
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dialkylaminopyridine-functionalized mesoporous silica nanosphere as an efficient and highly stable heterogeneous nucleophilic catalyst.
    Chen HT; Huh S; Wiench JW; Pruski M; Lin VS
    J Am Chem Soc; 2005 Sep; 127(38):13305-11. PubMed ID: 16173762
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Key role of the Lewis base position in asymmetric bifunctional catalysis: design and evaluation of a new ligand for chiral polymetallic catalysts.
    Fujimori I; Mita T; Maki K; Shiro M; Sato A; Furusho S; Kanai M; Shibasaki M
    J Am Chem Soc; 2006 Dec; 128(51):16438-9. PubMed ID: 17177358
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asymmetric acyl-transfer promoted by readily assembled chiral 4-N,N-dialkylaminopyridine derivatives.
    Dálaigh CO; Hynes SJ; O'Brien JE; McCabe T; Maher DJ; Watson GW; Connon SJ
    Org Biomol Chem; 2006 Jul; 4(14):2785-93. PubMed ID: 16826304
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The development of scalemic multidentate niobium complexes as catalysts for the highly stereoselective ring opening of meso-epoxides and meso-aziridines.
    Arai K; Lucarini S; Salter MM; Ohta K; Yamashita Y; Kobayashi S
    J Am Chem Soc; 2007 Jul; 129(26):8103-11. PubMed ID: 17567008
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Easily recyclable chiral polymeric Mn(III) salen complexes for oxidative kinetic resolution of racemic secondary alcohols.
    Kureshy RI; Ahmad I; Pathak K; Khan NU; Abdi SH; Prathap JK; Jasra RV
    Chirality; 2007 May; 19(5):352-7. PubMed ID: 17354262
    [TBL] [Abstract][Full Text] [Related]  

  • 20. P(i-PrNCH2CH2)3N as a Lewis base catalyst for the synthesis of beta-hydroxynitriles using TMSAN.
    Wadhwa K; Verkade JG
    J Org Chem; 2009 Aug; 74(15):5683-6. PubMed ID: 19555093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.