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Determination of the absolute configuration and evaluation of the in vitro antitumor activity of dilospirane B. <i>Phytochemistry Letters 5(4)</i>: 747-751. <a href=\"https://dx.doi.org/10.1016/j.phytol.2012.08.005\" target=\"_blank\">https://dx.doi.org/10.1016/j.phytol.2012.08.005</a>","BEntID":272719,"PublicFlag":1,"CheckedFlag":1,"wosflag":1,"vabbflag":0,"RefStringPartII":". <i>Phytochemistry Letters 5(4)</i>: 747-751. <a href=\"https://dx.doi.org/10.1016/j.phytol.2012.08.005\" target=\"_blank\">https://dx.doi.org/10.1016/j.phytol.2012.08.005</a>","DocTypID":8,"DocType":"Journal article","MarineFlag":1,"FreshFlag":0,"BrackishFlag":0,"TerrestrialFlag":0,"Authorstring":"Genta-Jouve, G.; Ioannou, E.; Mathieu, V.; Bruyère, C.; Lefranc, F.; Thomas, O.P.; Kiss, R.; Roussis, V.","OrigTitleTranslFlag":0,"Authorstringtrunc":"Genta-Jouve, G. <i>et al.</i>","Englishabstract":"The absolute configuration of dilospirane B (1), a diterpene featuring a novel carbon framework recently isolated from the brown alga <i>Dilophus spiralis</i>, was established on the basis of theoretical calculations of its electronic circular dichroism spectra applying the time-dependent density functional theory method. 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