BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 11767082)

  • 1. 1,6-Asymmetric induction during the conjugate addition of arylcopper reagents to a chiral sulfinyl-substituted pyrrolyl alpha,beta-unsaturated amide.
    Arai Y; Ueda K; Xie J; Masaki Y
    Chem Pharm Bull (Tokyo); 2001 Dec; 49(12):1609-14. PubMed ID: 11767082
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis of chiral sulfinyl-substituted 1-indolyl enones and asymmetric conjugate addition by an arylcopper reagent.
    Arai Y; Kasai M; Masaki Y
    Chem Pharm Bull (Tokyo); 2004 Jun; 52(6):733-8. PubMed ID: 15187397
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Highly enantioselective Cu(I)-Tol-BINAP-catalyzed asymmetric conjugate addition of Grignard reagents to α,β-unsaturated esters.
    Wang SY; Loh TP
    Chem Commun (Camb); 2010 Dec; 46(46):8694-703. PubMed ID: 21038042
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catalytic asymmetric conjugate addition of dialkylzinc reagents to beta-aryl-alpha,beta-unsaturated N-2,4,6-triisopropylphenylsulfonylaldimines with use of N-Boc-L-Val-connected amidophosphane-copper(I) catalyst.
    Soeta T; Kuriyama M; Tomioka K
    J Org Chem; 2005 Jan; 70(1):297-300. PubMed ID: 15624936
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted enones. Construction of all-carbon quaternary chiral centers.
    Martin D; Kehrli S; d'Augustin M; Clavier H; Mauduit M; Alexakis A
    J Am Chem Soc; 2006 Jul; 128(26):8416-7. PubMed ID: 16802804
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Addition of indolyl and pyrrolyl grignard reagents to 1-acylpyridinium salts.
    Kuethe JT; Comins DL
    J Org Chem; 2004 Apr; 69(8):2863-6. PubMed ID: 15074941
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Conjugate Addition of Grignard Reagents to Thiochromones Catalyzed by Copper Salts: A Unified Approach to Both 2-Alkylthiochroman-4-One and Thioflavanone.
    Bellinger TJ; Harvin T; Pickens-Flynn T; Austin N; Whitaker SH; Tang Yuk Tutein MLC; Hukins DT; Deese N; Guo F
    Molecules; 2020 May; 25(9):. PubMed ID: 32370080
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copper(I) catalyzed asymmetric 1,2-addition of Grignard reagents to α-methyl substituted α,β-unsaturated ketones.
    Madduri AV; Minnaard AJ; Harutyunyan SR
    Chem Commun (Camb); 2012 Feb; 48(10):1478-80. PubMed ID: 22124420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Enantioselective synthesis of chiral sulfones by Rh-catalyzed asymmetric addition of boronic acids to alpha,beta-unsaturated 2-pyridyl sulfones.
    Mauleón P; Alonso I; Rivero MR; Carretero JC
    J Org Chem; 2007 Dec; 72(26):9924-35. PubMed ID: 18047369
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly versatile enantioselective conjugate addition of Grignard reagents to alpha,beta-unsaturated thioesters.
    Ruiz BM; Geurts K; Fernández-Ibáñez MA; ter Horst B; Minnaard AJ; Feringa BL
    Org Lett; 2007 Nov; 9(24):5123-6. PubMed ID: 17975924
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cu-catalyzed asymmetric conjugate additions of dialkyl- and diarylzinc reagents to acyclic beta-silyl-alpha,beta-unsaturated ketones. Synthesis of allylsilanes in high diastereo- and enantiomeric purity.
    Kacprzynski MA; Kazane SA; May TL; Hoveyda AH
    Org Lett; 2007 Aug; 9(16):3187-90. PubMed ID: 17602643
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copper-catalyzed asymmetric allylic substitution with aryl and ethyl Grignard reagents.
    Selim KB; Yamada K; Tomioka K
    Chem Commun (Camb); 2008 Nov; (41):5140-2. PubMed ID: 18956048
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chiral aryl-copper(III) electrophiles: new opportunities in catalytic enantioselective arylations and domino processes.
    Rousseaux S; Vrancken E; Campagne JM
    Angew Chem Int Ed Engl; 2012 Oct; 51(44):10934-5. PubMed ID: 23001994
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Conjugate addition reactions of N-carbamoyl-4-pyridones with organometallic reagents.
    Dieter RK; Guo F
    J Org Chem; 2009 May; 74(10):3843-8. PubMed ID: 19366232
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sulfoxide-controlled S(N)2' displacements between cyanocuprates and epoxy vinyl sulfoxides.
    Marino JP; Anna LJ; Fernández de la Pradilla R; Martínez MV; Montero C; Viso A
    J Org Chem; 2000 Oct; 65(20):6462-73. PubMed ID: 11052089
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unprecedented copper-catalyzed asymmetric conjugate addition of organometallic reagents to alpha,beta-unsaturated lactams.
    Pineschi M; Del Moro F; Gini F; Minnaard AJ; Feringa BL
    Chem Commun (Camb); 2004 May; (10):1244-5. PubMed ID: 15136859
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A long-range chiral relay via tertiary amide group in asymmetric catalysis: new amino acid-derived N,P-ligands for copper-catalysed conjugate addition.
    Malkov AV; Hand JB; Kocovský P
    Chem Commun (Camb); 2003 Aug; (15):1948-9. PubMed ID: 12932047
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cyclopropylamines from N,N-dialkylcarboxamides and Grignard reagents in the presence of titanium tetraisopropoxide or methyltitanium triisopropoxide.
    de Meijere A; Chaplinski V; Winsel H; Kordes M; Stecker B; Gazizova V; Savchenko AI; Boese R; Schill F
    Chemistry; 2010 Dec; 16(46):13862-75. PubMed ID: 20945442
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Asymmetric copper-catalyzed conjugate additions of organometallic reagents in the syntheses of natural compounds and pharmaceuticals.
    Vargová D; Némethová I; Šebesta R
    Org Biomol Chem; 2020 May; 18(20):3780-3796. PubMed ID: 32391843
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Catalytic enantioselective 1,6-conjugate additions of propargyl and allyl groups.
    Meng F; Li X; Torker S; Shi Y; Shen X; Hoveyda AH
    Nature; 2016 Sep; 537(7620):387-393. PubMed ID: 27479320
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.