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 *

157 related articles for article (PubMed ID: 23649922)

  • 1. Tricycles by a new Ugi variation and Pictet-Spengler reaction in one pot.
    Sinha MK; Khoury K; Herdtweck E; Dömling A
    Chemistry; 2013 Jun; 19(25):8048-52. PubMed ID: 23649922
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expedient entry to the piperazinohydroisoquinoline ring system using a sequential Ugi/Pictet-Spengler/reductive methylation reaction protocol.
    Cano-Herrera MA; Miranda LD
    Chem Commun (Camb); 2011 Oct; 47(38):10770-2. PubMed ID: 21881642
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A versatile synthesis of pyrazolo[3,4-c]isoquinoline derivatives by reaction of 4-aryl-5-aminopyrazoles with aryl/heteroaryl aldehydes: the effect of the heterocycle on the reaction pathways.
    Bogza SL; Kobrakov KI; Malienko AA; Perepichka IF; Sujkov SY; Bryce MR; Lyubchik SB; Batsanov AS; Bogdan NM
    Org Biomol Chem; 2005 Mar; 3(5):932-40. PubMed ID: 15731881
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Stereoselective synthesis of 3-substituted tetrahydropyrazinoisoquinolines via intramolecular cyclization of enantiomerically enriched dihydro-2H-pyrazines.
    Reginato G; Catalani MP; Pezzati B; Di Fabio R; Bernardelli A; Curcuruto O; Moro E; Pozzan A; Mordini A
    Org Lett; 2015 Feb; 17(3):398-401. PubMed ID: 25629303
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Highly efficient solid-phase oxidative cleavage of olefins by OsO4-NalO4 in the intramolecular N-acyliminium Pictet-Spengler reaction.
    Nielsen TE; Meldal M
    Org Lett; 2005 Jun; 7(13):2695-8. PubMed ID: 15957924
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Beyond Pseudo-natural Products: Sequential Ugi/Pictet-Spengler Reactions Leading to Steroidal Pyrazinoisoquinolines That Trigger Caspase-Independent Death in HepG2 Cells.
    Alonso F; Galilea A; Mañez PA; Acebedo SL; Cabrera GM; Otero M; Barquero AA; Ramírez JA
    ChemMedChem; 2021 Jun; 16(12):1945-1955. PubMed ID: 33682316
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Regioselective, unconventional Pictet-Spengler cyclization strategy toward the synthesis of benzimidazole-linked imidazoquinoxalines on a soluble polymer support.
    Chen CH; Kuo J; Yellol GS; Sun CM
    Chem Asian J; 2011 Jun; 6(6):1557-65. PubMed ID: 21472995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polycyclic compounds by Ugi-Pictet-Spengler sequence.
    Wang W; Ollio S; Herdtweck E; Dömling A
    J Org Chem; 2011 Jan; 76(2):637-44. PubMed ID: 21190371
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of the tricyclic core in stemonamine alkaloids via one-pot gold(I)-catalyzed cyclization and schmidt rearrangement: formal synthesis of (±)-stemonamine.
    Kim C; Kang S; Rhee YH
    J Org Chem; 2014 Nov; 79(22):11119-24. PubMed ID: 25322172
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Total synthesis of cribrostatin 6.
    Knueppel D; Martin SF
    Angew Chem Int Ed Engl; 2009; 48(14):2569-71. PubMed ID: 19235818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis of H-pyrazolo[5,1-a]isoquinolines via copper(II)-catalyzed oxidation of an aliphatic C-H bond of tertiary amine in air.
    Li S; Wu J
    Org Lett; 2011 Feb; 13(4):712-5. PubMed ID: 21210650
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis of hexahydropyrrolo[2,1-a]isoquinoline compound libraries through a Pictet-Spengler cyclization/metal-catalyzed cross coupling/amidation sequence.
    Petersen R; Cohrt AE; Petersen MÅ; Wu P; Clausen MH; Nielsen TE
    Bioorg Med Chem; 2015 Jun; 23(11):2646-9. PubMed ID: 25703308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A convenient synthesis of 1,1-disubstituted 1,2,3,4-tetrahydroisoquinolines via Pictet-Spengler reaction using titanium(IV) isopropoxide and acetic-formic anhydride.
    Horiguchi Y; Kodama H; Nakamura M; Yoshimura T; Hanezi K; Hamada H; Saitoh T; Sano T
    Chem Pharm Bull (Tokyo); 2002 Feb; 50(2):253-7. PubMed ID: 11848218
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis of the tricyclic core of labiatin A and australin A.
    Clark JS; Vignard D; Parkin A
    Org Lett; 2011 Aug; 13(15):3980-3. PubMed ID: 21732661
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Solid-phase synthesis of pyrroloisoquinolines via the intramolecular N-acyliminium Pictet-Spengler reaction.
    Nielsen TE; Meldal M
    J Comb Chem; 2005; 7(4):599-610. PubMed ID: 16004504
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enantioselective synthesis of schulzeines B and C via a beta-lactone-derived surrogate for bishomoserine aldehyde.
    Liu G; Romo D
    Org Lett; 2009 Mar; 11(5):1143-6. PubMed ID: 19209875
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Pictet-Spengler Reaction Updates Its Habits.
    Calcaterra A; Mangiardi L; Delle Monache G; Quaglio D; Balducci S; Berardozzi S; Iazzetti A; Franzini R; Botta B; Ghirga F
    Molecules; 2020 Jan; 25(2):. PubMed ID: 31963860
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Preparation of hexahydrobenzo[f]isoquinolines using a vinylogous pictet-spengler cyclization.
    Cesati RR; Katzenellenbogen JA
    Org Lett; 2000 Nov; 2(23):3635-8. PubMed ID: 11073663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Asymmetric synthesis of the core structure of leucosceptroids A-D.
    Xie J; Ma Y; Horne DA
    J Org Chem; 2011 Aug; 76(15):6169-76. PubMed ID: 21644513
    [TBL] [Abstract][Full Text] [Related]  

  • 20. One-pot organocatalytic enantioselective domino double-Michael reaction and Pictet-Spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers.
    Hong BC; Liao WK; Dange NS; Liao JH
    Org Lett; 2013 Feb; 15(3):468-71. PubMed ID: 23311855
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.