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 *

147 related articles for article (PubMed ID: 20963247)

  • 1. Direct carbon-carbon bond formation via soft enolization: aldol addition of α-halogenated thioesters.
    Yost JM; Alfie RJ; Tarsis EM; Chong I; Coltart DM
    Chem Commun (Camb); 2011 Jan; 47(1):571-2. PubMed ID: 20963247
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Direct carbon-carbon bond formation via reductive soft enolization: a kinetically controlled syn-aldol addition of α-halo thioesters and enolizable aldehydes.
    Sauer SJ; Garnsey MR; Coltart DM
    J Am Chem Soc; 2010 Oct; 132(40):13997-9. PubMed ID: 20849119
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Overcoming the limitations of the Morita-Baylis-Hillman reaction: a rapid and general synthesis of alpha-alkenyl-beta'-hydroxy thioesters.
    Tarsis E; Gromova A; Lim D; Zhou G; Coltart DM
    Org Lett; 2008 Nov; 10(21):4819-22. PubMed ID: 18844367
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Asymmetric addition of dimethylzinc to alpha-ketoesters catalyzed by (-)-MITH.
    Wu HL; Wu PY; Shen YY; Uang BJ
    J Org Chem; 2008 Aug; 73(16):6445-7. PubMed ID: 18646857
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters.
    Sun J; Fu GC
    J Am Chem Soc; 2010 Apr; 132(13):4568-9. PubMed ID: 20222657
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Iridium-catalyzed C-C bond forming hydrogenation: direct regioselective reductive coupling of alkyl-substituted alkynes to activated ketones.
    Ngai MY; Barchuk A; Krische MJ
    J Am Chem Soc; 2007 Jan; 129(2):280-1. PubMed ID: 17212400
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Construction of contiguous tetrasubstituted chiral carbon stereocenters via direct catalytic asymmetric aldol and Mannich-type reactions.
    Matsunaga S; Yoshino T
    Chem Rec; 2011 Sep; 11(5):260-8. PubMed ID: 21898777
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Direct carbon-carbon bond formation via soft enolization: a biomimetic asymmetric Mannich reaction of phenylacetate thioesters.
    Kohler MC; Yost JM; Garnsey MR; Coltart DM
    Org Lett; 2010 Aug; 12(15):3376-9. PubMed ID: 20608684
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An exceptionally mild catalytic thioester aldol reaction inspired by polyketide biosynthesis.
    Lalic G; Aloise AD; Shair MD
    J Am Chem Soc; 2003 Mar; 125(10):2852-3. PubMed ID: 12617633
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A combined DFT and NMR investigation of the zinc organometallic intermediate proposed in the syn-selective tandem chain extension-aldol reaction of β-keto esters.
    Aiken KS; Eger WA; Williams CM; Spencer CM; Zercher CK
    J Org Chem; 2012 Jul; 77(14):5942-55. PubMed ID: 22703563
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Palladium-catalyzed synthesis of enantiomerically pure alpha-substituted allylboronic esters and their addition to aldehydes.
    Fernández E; Pietruszka J; Frey W
    J Org Chem; 2010 Aug; 75(16):5580-9. PubMed ID: 20672807
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Direct carbon-carbon bond formation via reductive soft enolization: a syn-selective Mannich addition of α-iodo thioesters.
    Truong N; Sauer SJ; Seraphin-Hatcher C; Coltart DM
    Org Biomol Chem; 2016 Aug; 14(33):7864-8. PubMed ID: 27492274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Asymmetric alkynylation of aldehydes with propiolates without high reagent loading and any additives.
    Kojima N; Nishijima S; Tsuge K; Tanaka T
    Org Biomol Chem; 2011 Jun; 9(12):4425-8. PubMed ID: 21552582
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tandem regio- and stereoselective organocuprate-mediated bis-allylic substitutions.
    Dieter RK; Guo F
    Org Lett; 2008 May; 10(10):2087-90. PubMed ID: 18422321
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A nickel catalyst for the addition of organoboronate esters to ketones and aldehydes.
    Bouffard J; Itami K
    Org Lett; 2009 Oct; 11(19):4410-3. PubMed ID: 19708680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Highly enantioselective synthesis of gamma-hydroxy-alpha,beta-acetylenic esters by asymmetric alkyne addition to aldehydes.
    Gao G; Wang Q; Yu XQ; Xie RG; Pu L
    Angew Chem Int Ed Engl; 2005 Dec; 45(1):122-5. PubMed ID: 16299819
    [No Abstract]   [Full Text] [Related]  

  • 19. Multi-component, regio-selective aldol addition of β-ketoesters to aldehydes: scope and applications.
    More V; Di Mola A; Croce G; Tedesco C; Petronzi C; Peduto A; De Caprariis P; Filosa R; Massa A
    Org Biomol Chem; 2011 Dec; 9(24):8483-8. PubMed ID: 22051978
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stereoselective synthesis of (Z)-alpha-halo-alpha,beta-unsaturated esters, and amides from aldehydes and trihaloesters or amides promoted by manganese.
    Concellón JM; Rodríguez-Solla H; Díaz P
    Org Biomol Chem; 2008 Feb; 6(3):451-3. PubMed ID: 18219412
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.