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Journal Abstract Search

264 related items for PubMed ID: 18226903

  • 1. Synthesis and stereochemistry of the terminal spiroketal domain of the phosphatase inhibitor dinophysistoxin-2.
    Forsyth CJ, Wang C.
    Bioorg Med Chem Lett; 2008 May 15; 18(10):3043-6. PubMed ID: 18226903
    [Abstract] [Full Text] [Related]

  • 2. Synthesis of the C1-C21 domain of azaspiracids-1 and -3.
    Zhang Z, Ding Y, Xu J, Chen Y, Forsyth CJ.
    Org Lett; 2013 May 17; 15(10):2338-41. PubMed ID: 23627769
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  • 3. Total synthesis and confirmation of the revised structures of azaspiracid-2 and azaspiracid-3.
    Nicolaou KC, Frederick MO, Petrovic G, Cole KP, Loizidou EZ.
    Angew Chem Int Ed Engl; 2006 Apr 10; 45(16):2609-15. PubMed ID: 16548033
    [No Abstract] [Full Text] [Related]

  • 4. Singlet oxygen-mediated synthesis of bis-spiroketals found in azaspiracids.
    Triantafyllakis M, Tofi M, Montagnon T, Kouridaki A, Vassilikogiannakis G.
    Org Lett; 2014 Jun 06; 16(11):3150-3. PubMed ID: 24869923
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  • 5. Stereoselective total synthesis of (-)-spirofungin A by utilising hydrogen-bond controlled spiroketalisation.
    Lynch JE, Zanatta SD, White JM, Rizzacasa MA.
    Chemistry; 2011 Jan 03; 17(1):297-304. PubMed ID: 21207625
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  • 7. A practical total synthesis of (+)-spirolaxine methyl ether.
    Yadav JS, Sreenivas M, Srinivas Reddy A, Subba Reddy BV.
    J Org Chem; 2010 Dec 03; 75(23):8307-10. PubMed ID: 21058660
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  • 8. Asymmetric synthesis of spiroketal, spiroether, and oxabicycle building blocks via stereoselective spiro- and bicycloannulation of 2-hydroxy dihydropyrans.
    Lejkowski M, Banerjee P, Runsink J, Gais HJ.
    Org Lett; 2008 Jul 03; 10(13):2713-6. PubMed ID: 18512930
    [Abstract] [Full Text] [Related]

  • 9. Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 by Total Synthesis and Comparative Analyses.
    Kenton NT, Adu-Ampratwum D, Okumu AA, McCarron P, Kilcoyne J, Rise F, Wilkins AL, Miles CO, Forsyth CJ.
    Angew Chem Int Ed Engl; 2018 Jan 15; 57(3):810-813. PubMed ID: 29193497
    [Abstract] [Full Text] [Related]

  • 10. Synthesis of the azaspiracid-1 trioxadispiroketal.
    Geisler LK, Nguyen S, Forsyth CJ.
    Org Lett; 2004 Nov 11; 6(23):4159-62. PubMed ID: 15524432
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  • 11. Synthesis of the ABCD trioxadispiroketal subunit of azaspiracid-1: an iodoetherification-dehydroiodination strategy for complex spiroketals.
    Li X, Li J, Mootoo DR.
    Org Lett; 2007 Oct 11; 9(21):4303-6. PubMed ID: 17880232
    [Abstract] [Full Text] [Related]

  • 12. Synthesis of the ABC fragment of the pectenotoxins.
    Halim R, Brimble MA, Merten J.
    Org Lett; 2005 Jun 23; 7(13):2659-62. PubMed ID: 15957915
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  • 14. Azaspiracid substituent at C1 is relevant to in vitro toxicity.
    Vilariño N, Nicolaou KC, Frederick MO, Cagide E, Alfonso C, Alonso E, Vieytes MR, Botana LM.
    Chem Res Toxicol; 2008 Sep 23; 21(9):1823-31. PubMed ID: 18707138
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  • 16. Synthetic studies towards the pectenotoxins: a review.
    Halim R, Brimble MA.
    Org Biomol Chem; 2006 Nov 21; 4(22):4048-58. PubMed ID: 17312955
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  • 19. Total synthesis of dinophysistoxin-2 and 2-epi-dinophysistoxin-2 and their PPase inhibition.
    Pang Y, Fang C, Twiner MJ, Miles CO, Forsyth CJ.
    Angew Chem Int Ed Engl; 2011 Aug 08; 50(33):7631-5. PubMed ID: 21726026
    [No Abstract] [Full Text] [Related]

  • 20. Synthesis and Enantiomeric Separation of a Novel Spiroketal Derivative: A Potent Human Telomerase Inhibitor with High in Vitro Anticancer Activity.
    Fuggetta MP, De Mico A, Cottarelli A, Morelli F, Zonfrillo M, Ulgheri F, Peluso P, Mannu A, Deligia F, Marchetti M, Roviello G, Reyes Romero A, Dömling A, Spanu P.
    J Med Chem; 2016 Oct 13; 59(19):9140-9149. PubMed ID: 27592503
    [Abstract] [Full Text] [Related]

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