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LITERATURE CITED

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    He J,Wang F,Polavarapu PL. Absolute configurations of chiral herbicides determined from vibrational circular dichroism. Chirality 2005; 17: S1S8.
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    Nafie LA. Vibrational circular dichroism: a new tool for the solution-state determination of the structure and absolute configuration of chiral natural product molecules. Nat Prod Commun 2008; 3: 451466.
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    Cichewicz RH,Clifford LJ,Lassen PR,Cao X,Freedman TB,Nafie LA,Deschamps JD,Kenyon VA,Flanary JR,Holman TR,Crews P. Stereochemical determination and bioactivity assessment of (S)-(+)-curcuphenol dimers isolated from the marine sponge Didiscus aceratus and synthesized through laccase biocatalysis. Bioorgan Med Chem 2005; 13: 56005612.
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    Keiderling TA, BerovaN, NakanishiK, WoodyRW, editors. Peptide and protein conformational studies with vibrational circular dichroism and related spectroscopies. Circular dichroism, principles and applications, 2nd ed. New York: Wiley; 2000. p 621666.
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    Taniguchi T,Monde K. Chiroptical analysis of glycoconjugates by vibrational circular dichroism. Trends Glycosci Glycotech 2007; 19: 149166.
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    Monde K,Taniguchi T,Miura N,Vairappan CS,Suzuki M. Absolute configurations of endoperoxides determined by vibrational circular dichroism (VCD). Tetrahedron Lett 2006; 47: 43894392.
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    Min HM,Aye M,Taniguchi T,Miura N,Monde K,Ohzawa K,Nikai T,Niwa M,Takaya Y. A structure and an absolute configuration of (+)-alternamin, a new coumarin from Murraya alternans having antidote activity against snake venom. Tetrahedron Lett 2007; 48: 61556158.
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