Zuber, Gérard Goldsmith, Michael-Rock Hopkins, Tamara D. Beratan, David N. Wipf, Peter Systematic Assignment of the Configuration of Flexible Natural Products by Spectroscopic and Computational Methods:  The Bistramide C Analysis The combination of NMR NOE, chemical shift, and <i>J</i>-coupling measurements with molar rotation and circular dichroism (CD) determinations, including RI-DFT BP86/aug-cc-pVDZ calculations, reduced a candidate pool of 1024 possible stereoisomers of (+)-bistramide C to a single absolute configuration assignment for the 10 stereogenic carbons of the marine natural product. Flexible Natural Products;calculation;chemical shift;stereoisomer;BP;measurement;Method;bistramide;marine;candidate pool;dichroism;Spectroscopic;configuration assignment;Configuration;combination;Bistramide C Analysis;10 stereogenic carbons;Systematic Assignment;determination;NMR NOE;Computational;molar rotation 2005-11-10
    https://acs.figshare.com/articles/journal_contribution/Systematic_Assignment_of_the_Configuration_of_Flexible_Natural_Products_by_Spectroscopic_and_Computational_Methods_The_Bistramide_C_Analysis/3258214
10.1021/ol052154v.s001