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250 related items for PubMed ID: 15976860

  • 1. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation.
    Paterson I, Chen DY, Coster MJ, Aceña JL, Bach J, Wallace DJ.
    Org Biomol Chem; 2005 Jul 07; 3(13):2431-40. PubMed ID: 15976860
    [Abstract] [Full Text] [Related]

  • 2. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment.
    Paterson I, Coster MJ, Chen DY, Aceña JL, Bach J, Keown LE, Trieselmann T.
    Org Biomol Chem; 2005 Jul 07; 3(13):2420-30. PubMed ID: 15976859
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and biological evaluation of spongistatin/altohyrtin analogues: E-ring dehydration and C46 side-chain truncation.
    Paterson I, Aceña JL, Bach J, Chen DY, Coster MJ.
    Chem Commun (Camb); 2003 Feb 21; (4):462-3. PubMed ID: 12638950
    [Abstract] [Full Text] [Related]

  • 4. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the AB-spiroacetal segment.
    Paterson I, Coster MJ, Chen DY, Oballa RM, Wallace DJ, Norcross RD.
    Org Biomol Chem; 2005 Jul 07; 3(13):2399-409. PubMed ID: 15976857
    [Abstract] [Full Text] [Related]

  • 5. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the CD-spiroacetal segment.
    Paterson I, Coster MJ, Chen DY, Gibson KR, Wallace DJ.
    Org Biomol Chem; 2005 Jul 07; 3(13):2410-9. PubMed ID: 15976858
    [Abstract] [Full Text] [Related]

  • 6. Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2).
    Heathcock CH, McLaughlin M, Medina J, Hubbs JL, Wallace GA, Scott R, Claffey MM, Hayes CJ, Ott GR.
    J Am Chem Soc; 2003 Oct 22; 125(42):12844-9. PubMed ID: 14558833
    [Abstract] [Full Text] [Related]

  • 7. Towards the combinatorial synthesis of spongistatin fragment libraries by using asymmetric aldol reactions on solid support.
    Paterson I, Gottschling D, Menche D.
    Chem Commun (Camb); 2005 Jul 28; (28):3568-70. PubMed ID: 16010326
    [Abstract] [Full Text] [Related]

  • 8. A modular approach to marine macrolide construction. 4. Assembly of C36-C51 and C29-C44 building blocks and evaluation of key coupling reactions targeting spongistatin 1 (altohyrtin A).
    Ciblat S, Kim J, Stewart CA, Wang J, Forgione P, Clyne D, Paquette LA.
    Org Lett; 2007 Feb 15; 9(4):719-22. PubMed ID: 17286379
    [Abstract] [Full Text] [Related]

  • 9. Synthesis and biological evaluation of 10,11-dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin.
    Paterson I, Gardner NM, Poullennec KG, Wright AE.
    J Nat Prod; 2008 Mar 15; 71(3):364-9. PubMed ID: 18081257
    [Abstract] [Full Text] [Related]

  • 10. Total synthesis and biological evaluation of (+)-neopeltolide and its analogues.
    Fuwa H, Saito A, Naito S, Konoki K, Yotsu-Yamashita M, Sasaki M.
    Chemistry; 2009 Nov 23; 15(46):12807-18. PubMed ID: 19882704
    [Abstract] [Full Text] [Related]

  • 11. Total synthesis and biological evaluation of potent analogues of dictyostatin: modification of the C2-C6 dienoate region.
    Paterson I, Gardner NM, Guzmán E, Wright AE.
    Bioorg Med Chem Lett; 2008 Dec 01; 18(23):6268-72. PubMed ID: 18951787
    [Abstract] [Full Text] [Related]

  • 12. Synthesis of the ABC tricyclic fragment of the pectenotoxins via stereocontrolled cyclization of a gamma-hydroxyepoxide appended to the AB spiroacetal unit.
    Halim R, Brimble MA, Merten J.
    Org Biomol Chem; 2006 Apr 07; 4(7):1387-99. PubMed ID: 16557329
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Total synthesis of (+)-spongistatin 1. An effective second-generation construction of an advanced EF Wittig salt, fragment union, and final elaboration.
    Smith AB, Zhu W, Shirakami S, Sfouggatakis C, Doughty VA, Bennett CS, Sakamoto Y.
    Org Lett; 2003 Mar 06; 5(5):761-4. PubMed ID: 12605509
    [Abstract] [Full Text] [Related]

  • 15. A second-generation synthesis of the C1-C28 portion of the altohyrtins (spongistatins).
    Hubbs JL, Heathcock CH.
    J Am Chem Soc; 2003 Oct 22; 125(42):12836-43. PubMed ID: 14558832
    [Abstract] [Full Text] [Related]

  • 16. The stereocontrolled total synthesis of spirastrellolide A methyl ester. Fragment coupling studies and completion of the synthesis.
    Paterson I, Anderson EA, Dalby SM, Lim JH, Maltas P.
    Org Biomol Chem; 2012 Aug 14; 10(30):5873-86. PubMed ID: 22504907
    [Abstract] [Full Text] [Related]

  • 17. The laulimalide family: total synthesis and biological evaluation of neolaulimalide, isolaulimalide, laulimalide and a nonnatural analogue.
    Gollner A, Altmann KH, Gertsch J, Mulzer J.
    Chemistry; 2009 Jun 08; 15(24):5979-97. PubMed ID: 19402092
    [Abstract] [Full Text] [Related]

  • 18. Short diastereoselective synthesis of the C1-C13 (AB spiroacetal) and C17-C28 fragments (CD spiroacetal) of spongistatin 1 and 2 through double chain-elongation reactions.
    Flowers CL, Vogel P.
    Chemistry; 2010 Dec 17; 16(47):14074-82. PubMed ID: 20963739
    [Abstract] [Full Text] [Related]

  • 19. Stereoselective synthesis of premisakinolide A, the monomeric counterpart of the marine 40-membered dimeric macrolide misakinolide A.
    Nakamura R, Tanino K, Miyashita M.
    Org Lett; 2005 Jul 07; 7(14):2929-32. PubMed ID: 15987172
    [Abstract] [Full Text] [Related]

  • 20. Total synthesis of apoptolidin: completion of the synthesis and analogue synthesis and evaluation.
    Nicolaou KC, Li Y, Sugita K, Monenschein H, Guntupalli P, Mitchell HJ, Fylaktakidou KC, Vourloumis D, Giannakakou P, O'Brate A.
    J Am Chem Soc; 2003 Dec 17; 125(50):15443-54. PubMed ID: 14664590
    [Abstract] [Full Text] [Related]

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