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Journal Abstract Search

123 related items for PubMed ID: 19807076

  • 1. New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: double-inversion approach.
    Kim DS, Dong CG, Kim JT, Guo H, Huang J, Tiseni PS, Kishi Y.
    J Am Chem Soc; 2009 Nov 04; 131(43):15636-41. PubMed ID: 19807076
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  • 4. Asymmetric Ni(II)/Cr(II)-mediated coupling reaction: stoichiometric process.
    Wan ZK, Choi HW, Kang FA, Nakajima K, Demeke D, Kishi Y.
    Org Lett; 2002 Dec 12; 4(25):4431-4. PubMed ID: 12465905
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  • 5. Total synthesis of halichondrin A, the missing member in the halichondrin class of natural products.
    Ueda A, Yamamoto A, Kato D, Kishi Y.
    J Am Chem Soc; 2014 Apr 02; 136(13):5171-6. PubMed ID: 24606005
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  • 7. Second generation synthesis of C27-C35 building block of E7389, a synthetic halichondrin analogue.
    Yang YR, Kim DS, Kishi Y.
    Org Lett; 2009 Oct 15; 11(20):4516-9. PubMed ID: 19754145
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  • 8. Catalytic enantioselective Cr-mediated propargylation: application to halichondrin synthesis.
    Liu S, Kim JT, Dong CG, Kishi Y.
    Org Lett; 2009 Oct 15; 11(20):4520-3. PubMed ID: 19810761
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  • 10. Halichondrin B: synthesis of a C1-C14 model via desymmetrization of (+)-conduritol E.
    Lambert WT, Burke SD.
    Org Lett; 2003 Feb 20; 5(4):515-8. PubMed ID: 12583757
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  • 11. Catalytic Ni/Cr-mediated macrocyclization without use of high-dilution techniques.
    Namba K, Kishi Y.
    J Am Chem Soc; 2005 Nov 09; 127(44):15382-3. PubMed ID: 16262397
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  • 13. Synthesis of the C20-C26 building block of halichondrins via a regiospecific and stereoselective S(N)2' reaction.
    Xie C, Nowak P, Kishi Y.
    Org Lett; 2002 Dec 12; 4(25):4427-9. PubMed ID: 12465904
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