BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 27176883)

  • 21. Organocatalytic, Enantioselective Synthesis of 1- and 3-Substituted Isochromans via Intramolecular Oxa-Michael Reaction of Alkoxyboronate: Synthesis of (+)-Sonepiprazole.
    Raveendra B; Maity S; Das BG; Ghorai P
    J Org Chem; 2015 Jul; 80(14):7008-18. PubMed ID: 26102523
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Direct enantioselective Michael addition of aldehydes to vinyl ketones catalyzed by chiral amines.
    Melchiorre P; Jørgensen KA
    J Org Chem; 2003 May; 68(11):4151-7. PubMed ID: 12762713
    [TBL] [Abstract][Full Text] [Related]  

  • 23. An Organocatalytic Highly Enantioselective Stereospecific Synthesis of 1,1-Disubstituted-1,3-Dihydroisobenzofurans.
    Kamilya C; Gorad SS; Ghorai P
    Chemistry; 2024 May; 30(25):e202303980. PubMed ID: 38391113
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Enantioselective synthesis of tetrahydrofuran spirooxindoles
    Shukla K; Khushboo ; Mahto P; Singh VK
    Org Biomol Chem; 2022 May; 20(20):4155-4160. PubMed ID: 35521781
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Direct asymmetric Michael addition of thioether-based aryl sulfanyl-propan-2-one to nitroalkenes catalyzed by a chiral amine-thiourea bifunctional organocatalyst.
    Jiang X; Zhang B; Zhang Y; Lin L; Yan W; Wang R
    Chirality; 2010 Jul; 22(7):625-34. PubMed ID: 20143410
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The highly enantioselective Michael addition of ketones to nitrodienes catalyzed by the efficient organocatalyst system of pyrrolidinyl-thioimidazole and chiral thioureido acid.
    Li ZB; Luo SP; Guo Y; Xia AB; Xu DQ
    Org Biomol Chem; 2010 Jun; 8(11):2505-8. PubMed ID: 20414483
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cinchona-based squaramide-catalysed cascade aza-Michael-Michael addition: enantioselective construction of functionalized spirooxindole tetrahydroquinolines.
    Yang W; Du DM
    Chem Commun (Camb); 2013 Oct; 49(78):8842-4. PubMed ID: 23959265
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Enantio- and Diastereoselective Synthesis of exo-Peroxyacetals: An Organocatalyzed Peroxyhemiacetalization/oxa-Michael Addition Cascade.
    Maity S; Parhi B; Ghorai P
    Angew Chem Int Ed Engl; 2016 Jun; 55(27):7723-7. PubMed ID: 26894663
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Asymmetric organocatalytic cascade reaction of aldehydes with 2-amino-β-nitrostyrenes: synthesis of chiral tetrahydroquinolines and dihydroquinolines.
    Lee Y; Kim SG
    J Org Chem; 2014 Sep; 79(17):8234-43. PubMed ID: 25098895
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An organocatalytic Michael-Michael cascade for the enantioselective construction of spirocyclopentane bioxindoles: control of four contiguous stereocenters.
    Sun W; Hong L; Zhu G; Wang Z; Wei X; Ni J; Wang R
    Org Lett; 2014 Jan; 16(2):544-7. PubMed ID: 24400909
    [TBL] [Abstract][Full Text] [Related]  

  • 31. An efficient organocatalytic method for highly enantioselective Michael addition of malonates to enones catalyzed by readily accessible primary amine-thiourea.
    Dudziński K; Pakulska AM; Kwiatkowski P
    Org Lett; 2012 Aug; 14(16):4222-5. PubMed ID: 22873407
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Organocatalytic Enantioselective Intramolecular Michael Addition by In Situ Generated Aminoisobenzofulvenes: Construction of Spiro Quaternary Carbon Stereocenters.
    Midya A; Khalse LD; Ghorai P
    Chemistry; 2023 Oct; 29(59):e202301563. PubMed ID: 37545475
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Organocatalytic, Enantioselective, Polarity-Matched Ring-Reorganization Domino Sequence Based on the 3-Oxindole Scaffold.
    Ren JW; Zheng L; Ye ZP; Deng ZX; Xie ZZ; Xiao JA; Zhu FW; Xiang HY; Chen XQ; Yang H
    Org Lett; 2019 Apr; 21(7):2166-2170. PubMed ID: 30908056
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Enantioselective organocatalytic conjugate addition of aldehydes to vinyl sulfones and vinyl phosphonates as challenging Michael acceptors.
    Sulzer-Mossé S; Alexakis A; Mareda J; Bollot G; Bernardinelli G; Filinchuk Y
    Chemistry; 2009; 15(13):3204-20. PubMed ID: 19204962
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Organocatalytic Asymmetric Mannich/Aza-Michael Cascade Reaction of δ-Formyl-α,β-unsaturated Ketones with Cyclic N-Sulfimines: Enantioselective Synthesis of Benzosulfamidate-Fused Pyrrolidines.
    Kim H; Kim Y; Kim SG
    J Org Chem; 2017 Aug; 82(15):8179-8185. PubMed ID: 28703582
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Chiral squaramide-catalyzed highly diastereo- and enantioselective direct Michael addition of nitroalkanes to nitroalkenes.
    Yang W; Du DM
    Chem Commun (Camb); 2011 Dec; 47(47):12706-8. PubMed ID: 22042378
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chiral primary amine catalyzed asymmetric Michael addition of malononitrile to α-substituted vinyl ketone.
    Fu N; Zhang L; Luo S
    Org Lett; 2015 Jan; 17(2):382-5. PubMed ID: 25551168
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Regioselective α-addition of vinylogous α-ketoester enolate in organocatalytic asymmetric Michael reactions: enantioselective synthesis of Rauhut-Currier type products.
    Weng Z; Zhou Y; Yue X; Jiang F; Guo W
    RSC Adv; 2022 Nov; 12(49):32056-32060. PubMed ID: 36415556
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Organocatalytic enantioselective Michael addition of a kojic acid derivative to nitro olefins.
    Wang J; Zhang Q; Zhang H; Feng Y; Yuan W; Zhang X
    Org Biomol Chem; 2012 Apr; 10(15):2950-4. PubMed ID: 22402616
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Diastereo- and Enantioselective Synthesis of Functionalized Dihydropyrans via an Organocatalytic Claisen Rearrangement/Oxa-Michael Addition Tandem Sequence.
    Li WC; Yang L; Wei ZL; Liao WW
    Org Lett; 2023 Sep; 25(34):6434-6439. PubMed ID: 37606692
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.