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Journal Abstract Search

409 related items for PubMed ID: 15816759

  • 1. Enantioselective synthesis of the C18-C25 segment of lasonolide A by an oxonia-cope prins cascade.
    Dalgard JE, Rychnovsky SD.
    Org Lett; 2005 Apr 14; 7(8):1589-91. PubMed ID: 15816759
    [Abstract] [Full Text] [Related]

  • 2. Stereoselective synthesis of the tetrahydropyran core of polycarvernoside A.
    Barry CS, Bushby N, Harding JR, Willis CL.
    Org Lett; 2005 Jun 23; 7(13):2683-6. PubMed ID: 15957921
    [Abstract] [Full Text] [Related]

  • 3. Oxonia-cope prins cyclizations: a facile method for the synthesis of tetrahydropyranones bearing quaternary centers.
    Dalgard JE, Rychnovsky SD.
    J Am Chem Soc; 2004 Dec 08; 126(48):15662-3. PubMed ID: 15571386
    [Abstract] [Full Text] [Related]

  • 4. Enantioselective total synthesis of macrolide antitumor agent (-)-lasonolide A.
    Ghosh AK, Gong G.
    Org Lett; 2007 Apr 12; 9(8):1437-40. PubMed ID: 17367152
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal.
    Marshall JA, Mulhearn JJ.
    Org Lett; 2005 Apr 14; 7(8):1593-6. PubMed ID: 15816760
    [Abstract] [Full Text] [Related]

  • 6. Prins cyclizations in silyl additives with suppression of epimerization: versatile tool in the synthesis of the tetrahydropyran backbone of natural products.
    Chan KP, Loh TP.
    Org Lett; 2005 Sep 29; 7(20):4491-4. PubMed ID: 16178566
    [Abstract] [Full Text] [Related]

  • 7. Stereoselective synthesis of both tetrahydropyran rings of the antitumor macrolide, (-)-lasonolide A.
    Ghosh AK, Ren GB.
    J Org Chem; 2012 Mar 02; 77(5):2559-65. PubMed ID: 22324913
    [Abstract] [Full Text] [Related]

  • 8. Total synthesis of (-)-exiguolide.
    Cook C, Guinchard X, Liron F, Roulland E.
    Org Lett; 2010 Feb 19; 12(4):744-7. PubMed ID: 20078080
    [Abstract] [Full Text] [Related]

  • 9. Total synthesis of potent antitumor agent (-)-lasonolide A: a cycloaddition-based strategy.
    Ghosh AK, Gong G.
    Chem Asian J; 2008 Oct 06; 3(10):1811-23. PubMed ID: 18712746
    [Abstract] [Full Text] [Related]

  • 10. An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A.
    Amans D, Bellosta V, Cossy J.
    Org Lett; 2007 Apr 12; 9(8):1453-6. PubMed ID: 17355145
    [Abstract] [Full Text] [Related]

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  • 12. 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
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  • 15. Concise and stereoselective synthesis of the N7-C25 fragment of psymberin.
    Rech JC, Floreancig PE.
    Org Lett; 2005 Nov 10; 7(23):5175-8. PubMed ID: 16268531
    [Abstract] [Full Text] [Related]

  • 16. Total Synthesis of (-)-Exiguolide.
    Zhang Z, Xie H, Li H, Gao L, Song Z.
    Org Lett; 2015 Oct 02; 17(19):4706-9. PubMed ID: 26371396
    [Abstract] [Full Text] [Related]

  • 17. Spongistatin synthetic studies. evolution of a scalable synthesis for the EF fragment of (+)-Spongistatin 1 exploiting a Petasis-Ferrier union/rearrangement tactic.
    Smith AB, Sfouggatakis C, Gotchev DB, Shirakami S, Bauer D, Zhu W, Doughty VA.
    Org Lett; 2004 Sep 30; 6(20):3637-40. PubMed ID: 15387567
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  • 19. Total synthesis, structural revision, and absolute configuration of (-)-clavosolide [corrected] A.
    Son JB, Kim SN, Kim NY, Lee DH.
    Org Lett; 2006 Feb 16; 8(4):661-4. PubMed ID: 16468736
    [Abstract] [Full Text] [Related]

  • 20. Total synthesis of a diastereomer of the marine natural product clavosolide A.
    Barry CS, Bushby N, Charmant JP, Elsworth JD, Harding JR, Willis CL.
    Chem Commun (Camb); 2005 Oct 28; (40):5097-9. PubMed ID: 16220183
    [Abstract] [Full Text] [Related]

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