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 *

127 related articles for article (PubMed ID: 20704315)

  • 21. New synthesis and evaluation of enantiomers of 7-methyl-2-exo-(3'-iodo-5'-pyridinyl)-7-azabicyclo[2.2.1]heptane as stereoselective ligands for PET imaging of nicotinic acetylcholine receptors.
    Gao Y; Horti AG; Kuwabara H; Ravert HT; Holt DP; Kumar A; Alexander M; Wong DF; Dannals RF
    Bioorg Med Chem Lett; 2008 Dec; 18(23):6168-70. PubMed ID: 18930397
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Studies towards the synthesis of bielschowskysin. Construction of the highly functionalized bicyclo[3.2.0]heptane segment.
    Jana A; Mondal S; Ghosh S
    Org Biomol Chem; 2015 Feb; 13(6):1846-59. PubMed ID: 25502963
    [TBL] [Abstract][Full Text] [Related]  

  • 23. First total synthesis and structural reassignment of (-)-aplysiallene.
    Wang J; Pagenkopf BL
    Org Lett; 2007 Aug; 9(18):3703-6. PubMed ID: 17691801
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Synthesis of microcin SF608.
    Valls N; Vallribera M; López-Canet M; Bonjoch J
    J Org Chem; 2002 Jul; 67(14):4945-50. PubMed ID: 12098309
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Synthesis of heterocyclic analogues of epibatidine via 7-azabicyclo[2.2.1]hept-2-yl radical intermediates. 1. Intermolecular reactions.
    Gómez-Sánchez E; Soriano E; Marco-Contelles J
    J Org Chem; 2008 Sep; 73(17):6784-92. PubMed ID: 18656981
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Effects of microcin SF608 and microcystin-LR, two cyanotobacterial compounds produced by Microcystis sp., on aquatic organisms.
    Wiegand C; Peuthert A; Pflugmacher S; Carmeli S
    Environ Toxicol; 2002; 17(4):400-6. PubMed ID: 12203963
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Rapid access to the tricyclic spirotetronic core of abyssomicins.
    Zografos AL; Yiotakis A; Georgiadis D
    Org Lett; 2005 Sep; 7(20):4515-8. PubMed ID: 16178572
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A practical synthesis of (+/-)-alpha-isosparteine from a tetraoxobispidine core.
    Blakemore PR; Kilner C; Norcross NR; Astles PC
    Org Lett; 2005 Oct; 7(21):4721-4. PubMed ID: 16209519
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Synthetic studies towards garsubellin A: synthesis of model systems and potential mimics by regioselective lithiation of bicyclo[3.3.1]nonane-2,4,9-trione derivatives from catechinic acid.
    Ahmad NM; Rodeschini V; Simpkins NS; Ward SE; Wilson C
    Org Biomol Chem; 2007 Jun; 5(12):1924-34. PubMed ID: 17551642
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mesoionic 1,3-oxazinium olates. rearrangement to acylketenes and 3-azabicyclo[3.1.1]heptanetriones.
    Sheibani H; Bernhardt PV; Wentrup C
    J Org Chem; 2005 Jul; 70(15):5859-61. PubMed ID: 16018678
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 3-{2-[Bis-(4-fluorophenyl)methoxy]ethyl}-6-substituted-3,6-diazabicyclo[3.1.1]heptanes as novel potent dopamine uptake inhibitors.
    Loriga G; Ruiu S; Manca I; Murineddu G; Dessi C; Pani L; Pinna GA
    Bioorg Med Chem; 2007 Jun; 15(11):3748-55. PubMed ID: 17399987
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Highly substituted oxabicyclic derivatives from furan: synthesis of (±)-platensimycin.
    Oblak EZ; Wright DL
    Org Lett; 2011 May; 13(9):2263-5. PubMed ID: 21452821
    [TBL] [Abstract][Full Text] [Related]  

  • 33. New carbocyclic nucleoside analogues with a bicyclo[2.2.1]heptane fragment as sugar moiety; synthesis, X-ray crystallography and anticancer activity.
    Tănase CI; Drăghici C; Căproiu MT; Shova S; Mathe C; Cocu FG; Enache C; Maganu M
    Bioorg Med Chem; 2014 Jan; 22(1):513-22. PubMed ID: 24280070
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Stereoselective synthesis of the C(1)-C(11) fragment of peloruside A.
    Owen RM; Roush WR
    Org Lett; 2005 Sep; 7(18):3941-4. PubMed ID: 16119937
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Au(I)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
    Vandavasi JK; Hu WP; Boominathan SS; Guo BC; Hsiao CT; Wang JJ
    Chem Commun (Camb); 2015 Aug; 51(62):12435-8. PubMed ID: 26145989
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Highly diastereoselective Diels-Alder reaction using a chiral auxiliary derived from levoglucosenone.
    Sarotti AM; Spanevello RA; Suárez AG
    Org Lett; 2006 Mar; 8(7):1487-90. PubMed ID: 16562923
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Synthetic study toward ecteinascidin 743: concise construction of the diazabicyclo[3.3.1]nonane skeleton and assembly of the pentacyclic core.
    Enomoto T; Yasui Y; Takemoto Y
    J Org Chem; 2010 Jul; 75(14):4876-9. PubMed ID: 20557114
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Unusual strain-releasing nucleophilic rearrangement of a bicyclo[2.2.1]heptane system to a cyclohexenyl derivative.
    Karimiahmadabadi M; Földesi A; Chattopadhyaya J
    J Org Chem; 2012 Nov; 77(21):9747-55. PubMed ID: 23062056
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Regio- and stereoselective ring openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene systems with copper catalyst-modified grignard reagents: application to the synthesis of an inhibitor of 5-lipoxygenase.
    Surman MD; Mulvihill MJ; Miller MJ
    J Org Chem; 2002 Jun; 67(12):4115-21. PubMed ID: 12054945
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Oxabicyclo[3.2.1]octenes in organic synthesis: direct ring opening of oxabicyclo[3.2.1] ring systems with diisobutylaluminum hydride and a silyl ketene acetal--synthesis of the chiral C(19)-C(26) and C(27)-C(32) fragments of Scytophycin C.
    Hunt KW; Grieco PA
    Org Lett; 2002 Jan; 4(2):245-8. PubMed ID: 11796061
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.