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 *

184 related articles for article (PubMed ID: 22898755)

  • 1. Substrate-controlled stereoselectivity in the Yamamoto aldol reaction.
    Schläger N; Kirschning A
    Org Biomol Chem; 2012 Oct; 10(38):7721-9. PubMed ID: 22898755
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Direct catalytic enantio- and diastereoselective aldol reaction of thioamides.
    Iwata M; Yazaki R; Chen IH; Sureshkumar D; Kumagai N; Shibasaki M
    J Am Chem Soc; 2011 Apr; 133(14):5554-60. PubMed ID: 21417332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study.
    Lee JM; Helquist P; Wiest O
    J Am Chem Soc; 2012 Sep; 134(36):14973-81. PubMed ID: 22891640
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Efficient organocatalytic cross-aldol reaction between aliphatic aldehydes through their functional differentiation.
    Kano T; Sugimoto H; Maruoka K
    J Am Chem Soc; 2011 Nov; 133(45):18130-3. PubMed ID: 21999103
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Asymmetric induction in hydrogen-mediated reductive aldol additions to alpha-amino aldehydes catalyzed by rhodium: selective formation of syn-stereotriads directed by intramolecular hydrogen-bonding.
    Jung CK; Krische MJ
    J Am Chem Soc; 2006 Dec; 128(51):17051-6. PubMed ID: 17177457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Primary amine-metal Lewis acid bifunctional catalysts based on a simple bidentate ligand: direct asymmetric aldol reaction.
    Daka P; Xu Z; Alexa A; Wang H
    Chem Commun (Camb); 2011 Jan; 47(1):224-6. PubMed ID: 20563349
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 1,5-asymmetric induction in boron-mediated beta-alkoxy methyl ketone aldol addition reactions.
    Evans DA; Côté B; Coleman PJ; Connell BT
    J Am Chem Soc; 2003 Sep; 125(36):10893-8. PubMed ID: 12952469
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Catalytic, asymmetric hypervinylogous Mukaiyama aldol reactions of extended furan-based silyl enolates.
    Curti C; Battistini L; Sartori A; Lodola A; Mor M; Rassu G; Pelosi G; Zanardi F; Casiraghi G
    Org Lett; 2011 Sep; 13(17):4738-41. PubMed ID: 21834551
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions.
    Ramasastry SS; Zhang H; Tanaka F; Barbas CF
    J Am Chem Soc; 2007 Jan; 129(2):288-9. PubMed ID: 17212404
    [No Abstract]   [Full Text] [Related]  

  • 10. Lewis base activation of Lewis acids: catalytic enantioselective glycolate aldol reactions.
    Denmark SE; Chung WJ
    Angew Chem Int Ed Engl; 2008; 47(10):1890-2. PubMed ID: 18236504
    [No Abstract]   [Full Text] [Related]  

  • 11. Rh-catalyzed aldehyde-aldehyde cross-aldol reaction under base-free conditions: in situ aldehyde-derived enolate formation through orthogonal activation.
    Lin L; Yamamoto K; Matsunaga S; Kanai M
    Chem Asian J; 2013 Dec; 8(12):2974-83. PubMed ID: 24108498
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Stereoselective titanium-mediated aldol reactions of a chiral isopropyl ketone.
    Zambrana J; Romea P; Urpí F
    Chem Commun (Camb); 2013 May; 49(40):4507-9. PubMed ID: 23576096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Oxazinanones as chiral auxiliaries: synthesis and evaluation in enolate alkylations and aldol reactions.
    Davies SG; Garner AC; Roberts PM; Smith AD; Sweet MJ; Thomson JE
    Org Biomol Chem; 2006 Jul; 4(14):2753-68. PubMed ID: 16826300
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lewis base-catalyzed conjugate reduction and reductive aldol reaction of alpha,beta-unsaturated ketones using trichlorosilane.
    Sugiura M; Sato N; Kotani S; Nakajima M
    Chem Commun (Camb); 2008 Sep; (36):4309-11. PubMed ID: 18802553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The vinylogous aldol reaction of unsaturated esters and enolizable aldehydes using the novel Lewis acid aluminum tris(2,6-di-2-naphthylphenoxide).
    Gazaille JA; Sammakia T
    Org Lett; 2012 Jun; 14(11):2678-81. PubMed ID: 22621176
    [TBL] [Abstract][Full Text] [Related]  

  • 16. General switch in regioselectivity in the Mukaiyama aldol reaction of silyloxyfuran with aldehydes in aqueous solvents.
    Woyciechowska M; Forcher G; Buda S; Mlynarski J
    Chem Commun (Camb); 2012 Nov; 48(89):11029-31. PubMed ID: 23037879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stereoselective synthesis of 1,3-anti diols by an Ipc-mediated domino aldol-coupling/reduction sequence.
    Dieckmann M; Menche D
    Org Lett; 2013 Jan; 15(1):228-31. PubMed ID: 23259690
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stereoselective synthesis of 1,4-diols by a tandem allylboration-allenylboration sequence.
    Zhao TS; Zhao J; Szabó KJ
    Org Lett; 2015 May; 17(9):2290-3. PubMed ID: 25898229
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Merging organocatalysis with transition metal catalysis: highly stereoselective α-alkylation of aldehydes.
    Xiao J
    Org Lett; 2012 Apr; 14(7):1716-9. PubMed ID: 22436110
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Picolylamine as an organocatalyst template for highly diastereo- and enantioselective aqueous aldol reactions.
    Nugent TC; Umar MN; Bibi A
    Org Biomol Chem; 2010 Sep; 8(18):4085-9. PubMed ID: 20623075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.