Complete 1H and 13C NMR structural assignments for five semi-synthetic eremantholides
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Five eremantholides were prepared from natural furanoheliangolides by reductions with Stryker's reagent, in previous works. We thus decided to perform a detailed and complete assignment of all 1H and 13C NMR data for those compounds. Through NMR experiments such as 1H NMR, 13C {1H} NMR, gCOSY, gHMQC, gHMBC, J-resolved, among others, it was achieved an unequivocal assignment of 1H and 13C NMR data for all studied substances, with measurement of all H/H homonuclear coupling constants and the clarification of all hydrogen signals multiplicities. Those data were not completely available yet in the literature.
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Eremantholides, Multiplicities clarifying, NMR data, Sesquiterpene lactones
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Inglês
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Journal of Molecular Structure, v. 1244.
