BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

291 related articles for article (PubMed ID: 29670061)

  • 1. Application of the Asymmetric Pictet-Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds.
    M Heravi M; Zadsirjan V; Malmir M
    Molecules; 2018 Apr; 23(4):. PubMed ID: 29670061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Organocatalytic enantioselective Pictet-Spengler approach to biologically relevant 1-benzyl-1,2,3,4-tetrahydroisoquinoline alkaloids.
    Ruiz-Olalla A; Würdemann MA; Wanner MJ; Ingemann S; van Maarseveen JH; Hiemstra H
    J Org Chem; 2015 May; 80(10):5125-32. PubMed ID: 25909585
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Organocatalytic enantioselective Pictet-Spengler reactions for the syntheses of 1-substituted 1,2,3,4-tetrahydroisoquinolines.
    Mons E; Wanner MJ; Ingemann S; van Maarseveen JH; Hiemstra H
    J Org Chem; 2014 Aug; 79(16):7380-90. PubMed ID: 25046801
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Development of the Pictet-Spengler reaction catalyzed by AuCl3/AgOTf.
    Youn SW
    J Org Chem; 2006 Mar; 71(6):2521-3. PubMed ID: 16526809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Chiral Pool in the Pictet-Spengler Reaction for the Synthesis of β-Carbolines.
    Dalpozzo R
    Molecules; 2016 May; 21(6):. PubMed ID: 27240334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Asymmetric synthesis of tetrahydroisoquinolines by enzymatic Pictet-Spengler reaction.
    Nishihachijo M; Hirai Y; Kawano S; Nishiyama A; Minami H; Katayama T; Yasohara Y; Sato F; Kumagai H
    Biosci Biotechnol Biochem; 2014; 78(4):701-7. PubMed ID: 25036970
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles.
    Pulka K
    Curr Opin Drug Discov Devel; 2010; 13(6):669-84. PubMed ID: 21061230
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enantioselective Synthesis of Hydantoin and Diketopiperazine-Fused Tetrahydroisoquinolines via Pictet-Spengler Reaction.
    Liu SI; Haung JY; Barve IJ; Huang SC; Sun CM
    ACS Comb Sci; 2019 Apr; 21(4):336-344. PubMed ID: 30839194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Catalytic Asymmetric Pictet-Spengler Platform as a Biomimetic Diversification Strategy toward Naturally Occurring Alkaloids.
    Scharf MJ; List B
    J Am Chem Soc; 2022 Aug; 144(34):15451-15456. PubMed ID: 35976162
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A suitable preparation of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines and their ring homologs with a reusable Preyssler heteropolyacid as catalyst.
    Romanelli GP; Ruiz DM; Autino JC; Giaccio HE
    Mol Divers; 2010 Nov; 14(4):803-7. PubMed ID: 19572201
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Research progress of Pictet-Spenglerases].
    Xie Y; Chen Q; Zhang S; Shen C
    Sheng Wu Gong Cheng Xue Bao; 2020 Oct; 36(10):2001-2016. PubMed ID: 33169566
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pictet-Spenglerases in alkaloid biosynthesis: Future applications in biocatalysis.
    Roddan R; Ward JM; Keep NH; Hailes HC
    Curr Opin Chem Biol; 2020 Apr; 55():69-76. PubMed ID: 31978651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Solid-phase synthesis of tetrahydro-beta-carbolines and tetrahydroisoquinolines by stereoselective intramolecular N-carbamyliminium Pictet-Spengler reactions.
    Diness F; Beyer J; Meldal M
    Chemistry; 2006 Oct; 12(31):8056-66. PubMed ID: 16881029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Pictet-Spengler reaction in solid-phase combinatorial chemistry.
    Nielsen TE; Diness F; Meldal M
    Curr Opin Drug Discov Devel; 2003 Nov; 6(6):801-14. PubMed ID: 14758752
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exploring the Chemistry of Spiroindolenines by Mechanistically-Driven Reaction Development: Asymmetric Pictet-Spengler-type Reactions and Beyond.
    Zheng C; You SL
    Acc Chem Res; 2020 Apr; 53(4):974-987. PubMed ID: 32275392
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enzymatic and Chemoenzymatic Three-Step Cascades for the Synthesis of Stereochemically Complementary Trisubstituted Tetrahydroisoquinolines.
    Erdmann V; Lichman BR; Zhao J; Simon RC; Kroutil W; Ward JM; Hailes HC; Rother D
    Angew Chem Int Ed Engl; 2017 Oct; 56(41):12503-12507. PubMed ID: 28727894
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Collective synthesis of natural products by means of organocascade catalysis.
    Jones SB; Simmons B; Mastracchio A; MacMillan DW
    Nature; 2011 Jul; 475(7355):183-8. PubMed ID: 21753848
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interfacing Whole Cell Biocatalysis with a Biocompatible Pictet-Spengler Reaction for One-Pot Syntheses of Tetrahydroisoquinolines and Tryptolines.
    Andersen CM; Knudson LD; Domaille DW
    Chembiochem; 2023 Dec; 24(24):e202300464. PubMed ID: 37801398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Asymmetric total synthesis of (-)-jorunnamycins A and C and (-)-jorumycin from L-tyrosine.
    Chen R; Liu H; Chen X
    J Nat Prod; 2013 Sep; 76(9):1789-95. PubMed ID: 24070054
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel Lewis acid catalyzed [3 + 3]-annulation strategy for the syntheses of tetrahydro-β-carbolines and tetrahydroisoquinolines.
    Wang S; Chai Z; Zhou S; Wang S; Zhu X; Wei Y
    Org Lett; 2013 Jun; 15(11):2628-31. PubMed ID: 23662783
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.