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 *

135 related articles for article (PubMed ID: 12182597)

  • 1. A divergent approach to the myriaporones and tedanolide: completion of the carbon skeleton of myriaporone 1.
    Taylor RE; Hearn BR; Ciavarri JP
    Org Lett; 2002 Aug; 4(17):2953-5. PubMed ID: 12182597
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis of simplified tedanolide analogues--connecting tedanolide to myriaporone and gephyronic acid.
    Diaz N; Naini A; Muthukumar Y; Sasse F; Kalesse M
    ChemMedChem; 2012 May; 7(5):771-5. PubMed ID: 22383258
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthetic studies of tedanolide, a marine macrolide displaying potent antitumor activity. Stereoselective synthesis of the C13-C23 segment.
    Iwata Y; Tanino K; Miyashita M
    Org Lett; 2005 Jun; 7(12):2341-4. PubMed ID: 15932193
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Studies on the synthesis of tedanolide. 2. Stereoselective synthesis of a protected C(1)-C(12) fragment.
    Roush WR; Newcom JS
    Org Lett; 2002 Dec; 4(26):4739-42. PubMed ID: 12489975
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Divergent and stereocontrolled synthesis of the enamide side chains of oximidines I/II/III, salicylihalamides A/B, lobatamides A/D, and CJ-12,950.
    Coleman RS; Liu PH
    Org Lett; 2004 Feb; 6(4):577-80. PubMed ID: 14961627
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Control of olefin geometry in the bryostatin B-ring through exploitation of a C(2)-symmetry breaking tactic and a Smith-Tietze coupling reaction.
    Hale KJ; Hummersone MG; Bhatia GS
    Org Lett; 2000 Jul; 2(15):2189-92. PubMed ID: 10930240
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A.
    Amans D; Bellosta V; Cossy J
    Org Lett; 2007 Apr; 9(8):1453-6. PubMed ID: 17355145
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Total synthesis of (+)-oocydin A: application of the Suzuki-Miyaura cross-coupling of 1,1-dichloro-1-alkenes with 9-alkyl 9-BBN.
    Roulland E
    Angew Chem Int Ed Engl; 2008; 47(20):3762-5. PubMed ID: 18399555
    [No Abstract]   [Full Text] [Related]  

  • 9. A unified approach to the tedanolides: total synthesis of (+)-13-deoxytedanolide.
    Smith AB; Adams CM; Barbosa SA; Degnan AP
    Proc Natl Acad Sci U S A; 2004 Aug; 101(33):12042-7. PubMed ID: 15163795
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Total synthesis of (+)-tedanolide.
    Smith AB; Lee D
    J Am Chem Soc; 2007 Sep; 129(35):10957-62. PubMed ID: 17691787
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Myriaporone 3/4 structure--activity relationship studies define a pharmacophore targeting eukaryotic protein synthesis.
    Hines J; Roy M; Cheng H; Agapakis CM; Taylor R; Crews CM
    Mol Biosyst; 2006 Aug; 2(8):371-9. PubMed ID: 16880957
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Studies on the synthesis of tedanolide: synthesis of the C(5)-C(21) segment via a highly stereoselective fragment assembly aldol reaction of a chiral beta,gamma-unsaturated methyl ketone.
    Roush WR; Lane GC
    Org Lett; 1999 Jul; 1(1):95-8. PubMed ID: 10822542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthetic studies on bioactive natural polyketides: intramolecular nitrile oxide-olefin cycloaddition approach for construction of a macrolactone skeleton of macrosphelide B.
    Paek SM; Suh YG
    Molecules; 2011 Jun; 16(6):4850-60. PubMed ID: 21666551
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Anti aldol selectivity in a synthetic approach to the C1-C12 fragment of the tedanolides.
    Jung ME; Zhang TH
    Org Lett; 2008 Jan; 10(1):137-40. PubMed ID: 18067310
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach.
    Jung ME; Yoo D
    Org Lett; 2007 Aug; 9(18):3543-6. PubMed ID: 17676748
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Toward the synthesis of peloruside a: fragment synthesis and coupling studies.
    Paterson I; Di Francesco ME; Kühn T
    Org Lett; 2003 Feb; 5(4):599-602. PubMed ID: 12583779
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spongistatin synthetic studies. An efficient, second-generation construction of an advanced ABCD intermediate.
    Smith AB; Doughty VA; Sfouggatakis C; Bennett CS; Koyanagi J; Takeuchi M
    Org Lett; 2002 Mar; 4(5):783-6. PubMed ID: 11869127
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stereoselective synthesis of the C1-C13 fragment of (+)-discodermolide using asymmetric allyltitanations.
    BouzBouz S; Cossy J
    Org Lett; 2003 Aug; 5(17):3029-31. PubMed ID: 12916973
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Synthesis of the C12-C19 fragment of (+)-peloruside A through a diastereomer-discriminating RCM reaction.
    Roulland E; Ermolenko MS
    Org Lett; 2005 May; 7(11):2225-8. PubMed ID: 15901175
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Total synthesis of the novel antifungal agent (+/-)-jesterone.
    Mehta G; Pan SC
    Org Lett; 2004 Mar; 6(5):811-3. PubMed ID: 14986981
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.