BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

327 related articles for article (PubMed ID: 28796165)

  • 41. Asymmetric Michael addition of ketones to nitroolefins: pyrrolidinyl-oxazole-carboxamides as new efficient organocatalysts.
    Kamal A; Sathish M; Srinivasulu V; Chetna J; Chandra Shekar K; Nekkanti S; Tangella Y; Shankaraiah N
    Org Biomol Chem; 2014 Oct; 12(40):8008-18. PubMed ID: 25181422
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Catalytic asymmetric synthesis of α,β-disubstituted α,γ-diaminophosphonic acid precursors by Michael addition of α-substituted nitrophosphonates to nitroolefins.
    Tripathi CB; Kayal S; Mukherjee S
    Org Lett; 2012 Jul; 14(13):3296-9. PubMed ID: 22702411
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation.
    Sulzer-Mossé S; Alexakis A
    Chem Commun (Camb); 2007 Aug; (30):3123-35. PubMed ID: 17653365
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water.
    Zhu S; Yu S; Ma D
    Angew Chem Int Ed Engl; 2008; 47(3):545-8. PubMed ID: 18038442
    [No Abstract]   [Full Text] [Related]  

  • 45. Highly stereoselective [4+2] and [3+2] spiroannulations of 2-(2-oxoindolin-3-ylidene)acetic esters catalyzed by bifunctional thioureas.
    Monari M; Montroni E; Nitti A; Lombardo M; Trombini C; Quintavalla A
    Chemistry; 2015 Jul; 21(31):11038-49. PubMed ID: 26032428
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Asymmetric Michael reactions catalyzed by a highly efficient and recyclable quaternary ammonium ionic liquid-supported organocatalyst in aqueous media.
    Ghosh SK; Qiao Y; Ni B; Headley AD
    Org Biomol Chem; 2013 Mar; 11(11):1801-4. PubMed ID: 23381599
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Highly efficient asymmetric Michael addition of aldehyde to nitroolefin using perhydroindolic acid as a chiral organocatalyst.
    Zhao L; Shen J; Liu D; Liu Y; Zhang W
    Org Biomol Chem; 2012 Apr; 10(14):2840-6. PubMed ID: 22388774
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A new entry to cascade organocatalysis: reactions of stable sulfur ylides and nitroolefins sequentially catalyzed by thiourea and DMAP.
    Lu LQ; Cao YJ; Liu XP; An J; Yao CJ; Ming ZH; Xiao WJ
    J Am Chem Soc; 2008 Jun; 130(22):6946-8. PubMed ID: 18473466
    [TBL] [Abstract][Full Text] [Related]  

  • 49. New bifunctional 1,3-diamine organocatalysts derived from (+)-camphoric acid for asymmetric Michael addition of 1,3-dicarbonyl compounds to nitroolefins.
    Rénio M; Murtinho D; Ventura MR
    Chirality; 2022 May; 34(5):782-795. PubMed ID: 35166402
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Asymmetric Michael additions of α-nitrocyclohexanone to aryl nitroalkenes catalyzed by natural amino acid-derived bifunctional thioureas.
    Jörres M; Schiffers I; Atodiresei I; Bolm C
    Org Lett; 2012 Sep; 14(17):4518-21. PubMed ID: 22928812
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst.
    Bernardi L; Fochi M
    Molecules; 2016 Jul; 21(8):. PubMed ID: 27483233
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A new synthetic route for axially chiral secondary amines with binaphthyl backbone and their applications in asymmetric Michael reaction of aldehydes to nitroalkenes.
    Liang DC; Luo RS; Yin LH; Chan AS; Lu G
    Org Biomol Chem; 2012 Apr; 10(15):3071-9. PubMed ID: 22395306
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A simple primary amine thiourea catalyzed highly enantioselective conjugate addition of alpha,alpha-disubstituted aldehydes to maleimides.
    Xue F; Liu L; Zhang S; Duan W; Wang W
    Chemistry; 2010 Jul; 16(27):7979-82. PubMed ID: 20540054
    [No Abstract]   [Full Text] [Related]  

  • 54. Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins--a rational approach.
    Wiesner M; Revell JD; Wennemers H
    Angew Chem Int Ed Engl; 2008; 47(10):1871-4. PubMed ID: 18228232
    [No Abstract]   [Full Text] [Related]  

  • 55. Enantioselective Michael reactions of beta, beta-disubstituted nitroalkenes: a new approach to beta(2,2)-amino acids with hetero-quaternary stereocenters.
    Lu HH; Zhang FG; Meng XG; Duan SW; Xiao WJ
    Org Lett; 2009 Sep; 11(17):3946-9. PubMed ID: 19653671
    [TBL] [Abstract][Full Text] [Related]  

  • 56. An asymmetric Michael addition of α,α-disubstituted aldehydes to maleimides leading to a one-pot enantioselective synthesis of lactones catalyzed by amino acids.
    Kokotos CG
    Org Lett; 2013 May; 15(10):2406-9. PubMed ID: 23627257
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Organocatalytic and direct asymmetric vinylogous Michael addition of alpha,alpha-dicyanoolefins to alpha,beta-unsaturated aldehydes.
    Xie JW; Yue L; Xue D; Ma XL; Chen YC; Wu Y; Zhu J; Deng JG
    Chem Commun (Camb); 2006 Apr; (14):1563-5. PubMed ID: 16575461
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Adapting to substrate challenges: peptides as catalysts for conjugate addition reactions of aldehydes to α,β-disubstituted nitroolefins.
    Duschmalé J; Wennemers H
    Chemistry; 2012 Jan; 18(4):1111-20. PubMed ID: 22189758
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Highly enantioselective Michael addition promoted by a new diterpene-derived bifunctional thiourea catalyst: a doubly stereocontrolled approach to chiral succinimide derivatives.
    Song ZT; Zhang T; Du HL; Ma ZW; Zhang CH; Tao JC
    Chirality; 2014 Feb; 26(2):121-7. PubMed ID: 24420919
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Asymmetric organocatalytic formal aza-Michael addition of ammonia to nitroalkenes.
    Lykke L; Monge D; Nielsen M; Jørgensen KA
    Chemistry; 2010 Dec; 16(45):13330-4. PubMed ID: 21038334
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.