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 *

243 related articles for article (PubMed ID: 16805544)

  • 1. High chelation control of three contiguous stereogenic centers in the Reformatsky reactions of indium enolates with alpha-hydroxy ketones: unexpected stereochemistry of lactone formation.
    Babu SA; Yasuda M; Okabe Y; Shibata I; Baba A
    Org Lett; 2006 Jul; 8(14):3029-32. PubMed ID: 16805544
    [TBL] [Abstract][Full Text] [Related]  

  • 2. In- or In(I)-employed tailoring of the stereogenic centers in the Reformatsky-type reactions of simple ketones, alpha-alkoxy ketones, and beta-keto esters.
    Babu SA; Yasuda M; Shibata I; Baba A
    J Org Chem; 2005 Dec; 70(25):10408-19. PubMed ID: 16323851
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Regio- and diastereoselective rhodium-catalyzed allylic substitution with acyclic alpha-alkoxy-substituted copper(I) enolates: stereodivergent approach to 2,3,6-trisubstituted dihydropyrans.
    Evans PA; Lawler MJ
    J Am Chem Soc; 2004 Jul; 126(28):8642-3. PubMed ID: 15250703
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In- or in(I)-employed diastereoselective Reformatsky-type reactions with ketones: 1H NMR investigations on the active species.
    Babu SA; Yasuda M; Shibata I; Baba A
    Org Lett; 2004 Nov; 6(24):4475-8. PubMed ID: 15548054
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Conjugate additions of cyclic oxygen-bound nickel enolates to alpha,beta-unsaturated ketones.
    Maya CM; Cámpora J; Carmona E; Matas I; Palma P; Gutiérrez-Puebla E; Monge A
    Chemistry; 2007; 13(13):3675-87. PubMed ID: 17253649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Highly diastereoselective Michael addition of alpha-hydroxy acid derivatives and enantioselective synthesis of (+)-crobarbatic acid.
    Jang DP; Chang JW; Uang BJ
    Org Lett; 2001 Apr; 3(7):983-5. PubMed ID: 11277775
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ti-catalyzed reformatsky-type coupling between alpha-halo ketones and aldehydes.
    Estévez RE; Paradas M; Millan A; Jiménez T; Robles R; Cuerva JM; Oltra JE
    J Org Chem; 2008 Feb; 73(4):1616-9. PubMed ID: 18189411
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coupling reaction of alkyl chlorides with silyl enolates catalyzed by indium trihalide.
    Nishimoto Y; Yasuda M; Baba A
    Org Lett; 2007 Nov; 9(24):4931-4. PubMed ID: 17975916
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ylide-initiated michael addition-cyclization reactions beyond cyclopropanes.
    Sun XL; Tang Y
    Acc Chem Res; 2008 Aug; 41(8):937-48. PubMed ID: 18656968
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly diastereoselective catalytic Meerwein-Ponndorf-Verley reductions.
    Yin J; Huffman MA; Conrad KM; Armstrong JD
    J Org Chem; 2006 Jan; 71(2):840-3. PubMed ID: 16409008
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Indium-promoted Reformatsky reaction: a straightforward access to β-amino and β-hydroxy α,α-difluoro carbonyl compounds.
    Poisson T; Belhomme MC; Pannecoucke X
    J Org Chem; 2012 Oct; 77(20):9277-85. PubMed ID: 22998653
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reactive barium-promoted Reformatsky-type reaction of alpha-chloroketones with aldehydes.
    Yanagisawa A; Takahashi H; Arai T
    Chem Commun (Camb); 2004 Mar; (5):580-1. PubMed ID: 14973617
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Highly enantio- and diastereoselective Brassard type hetero-Diels-Alder approach to 5-methyl-containing alpha,beta-unsaturated delta-lactones.
    Lin L; Fan Q; Qin B; Feng X
    J Org Chem; 2006 May; 71(11):4141-6. PubMed ID: 16709053
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Alpha,alpha-disubstituted boron enolates in the asymmetric synthesis of quaternary carbon centers.
    Burke ED; Gleason JL
    Org Lett; 2004 Feb; 6(3):405-7. PubMed ID: 14748604
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Construction of a chiral quaternary carbon center by indium-catalyzed asymmetric alpha-alkenylation of beta-ketoesters.
    Fujimoto T; Endo K; Tsuji H; Nakamura M; Nakamura E
    J Am Chem Soc; 2008 Apr; 130(13):4492-6. PubMed ID: 18331035
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recent advances in the diastereoselective Reformatsky-type reaction.
    Choppin S; Ferreiro-Medeiros L; Barbarotto M; Colobert F
    Chem Soc Rev; 2013 Feb; 42(3):937-49. PubMed ID: 23212078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis of C13-C25 fragment of 24-demethylbafilomycin C(1) via diastereoselective aldol reactions of a ketone boron enolate as the key step.
    Guan Y; Wu J; Sun L; Dai WM
    J Org Chem; 2007 Jun; 72(13):4953-60. PubMed ID: 17518500
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Development of diastereoselective birch reduction-alkylation reactions of bi- and tricyclic beta-alkoxy-alpha,beta-unsaturated ketones.
    Hiroya K; Ichihashi Y; Furutono A; Inamoto K; Sakamoto T; Doi T
    J Org Chem; 2009 Sep; 74(17):6623-30. PubMed ID: 19658421
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diastereoselective addition of gamma-substituted allylic nucleophiles to ketones: highly stereoselective synthesis of tertiary homoallylic alcohols using an allylic tributylstannane/stannous chloride system.
    Yasuda M; Hirata K; Nishino M; Yamamoto A; Baba A
    J Am Chem Soc; 2002 Nov; 124(45):13442-7. PubMed ID: 12418896
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Asymmetric silaboration of terminal allenes bearing alpha-stereogenic centers: stereoselection based on "reagent control".
    Ohmura T; Suginome M
    Org Lett; 2006 Jun; 8(12):2503-6. PubMed ID: 16737299
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.