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Journal Abstract Search

151 related items for PubMed ID: 20161196

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  • 2. Spongipyran Synthetic Studies. Evolution of a Scalable Total Synthesis of (+)-Spongistatin 1.
    Smith AB, Sfouggatakis C, Risatti CA, Sperry JB, Zhu W, Doughty VA, Tomioka T, Gotchev DB, Bennett CS, Sakamoto S, Atasoylu O, Shirakami S, Bauer D, Takeuchi M, Koyanagi J, Sakamoto Y.
    Tetrahedron; 2009 Sep 15; 65(33):6489-6509. PubMed ID: 20640040
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  • 3. 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
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  • 4. Gram-scale synthesis of (+)-spongistatin 1: development of an improved, scalable synthesis of the F-ring subunit, fragment union, and final elaboration.
    Smith AB, Tomioka T, Risatti CA, Sperry JB, Sfouggatakis C.
    Org Lett; 2008 Oct 02; 10(19):4359-62. PubMed ID: 18754594
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  • 9. Synthesis of the C-1-C-28 ABCD unit of spongistatin 1.
    Gaunt MJ, Jessiman AS, Orsini P, Tanner HR, Hook DF, Ley SV.
    Org Lett; 2003 Dec 11; 5(25):4819-22. PubMed ID: 14653682
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  • 10. 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
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  • 11. 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
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  • 12. 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
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  • 13. Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals.
    Holson EB, Roush WR.
    Org Lett; 2002 Oct 17; 4(21):3723-5. PubMed ID: 12375928
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  • 14. Spirastrellolide Studies. Synthesis of the C(1)-C(25) Southern Hemispheres of Spirastrellolides A and B, Exploiting Anion Relay Chemistry.
    Smith AB, Smits H, Kim DS.
    Tetrahedron; 2010 Aug 14; 66(33):6597-6605. PubMed ID: 20694174
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  • 15. 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
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  • 18. 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
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  • 19. A convergent total synthesis of (±)-γ-rubromycin.
    Wu KL, Mercado EV, Pettus TR.
    J Am Chem Soc; 2011 Apr 27; 133(16):6114-7. PubMed ID: 21452818
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