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- W2161330331 abstract "A complete analysis of 1H and 13C NMR spectra of the trypanocidal sesquiterpene lactone eremantholide C and two of its analogues is described. These structurally similar sesquiterpene lactones were submitted to 1H NMR, 13C {1H} NMR, gCOSY, gHSQC, gHMBC, J-resolved and DPFGSE-NOE NMR techniques. The detailed analysis of those results, correlated to some computational calculations (molecular mechanics), led to the total and unequivocal assignment of all 1H and 13C NMR data. The determination of all 1H/1H coupling constants and all signal multiplicities, together with the elimination of previous ambiguities were also achieved. Copyright © 2008 John Wiley & Sons, Ltd." @default.
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- W2161330331 date "2008-01-01" @default.
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- W2161330331 title "Detailed1H and13C NMR structural assignment and relative stereochemistry determination for three closely related sesquiterpene lactones" @default.
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- W2161330331 doi "https://doi.org/10.1002/mrc.2220" @default.
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