A divergent approach to the 7-oxa (-)-muricatacin analogue 2, the corresponding (+)-enantiomer ent-2 and the furanolactone 3 is reported starting from d-xylose. The resulting lactones have shown a potent and selective in vitro cytotoxicity against certain human neoplastic cell lines. © 2006 Elsevier Masson SAS. All rights reserved.
CITATION STYLE
Popsavin, V., Srećo, B., Krstić, I., Popsavin, M., Kojić, V., & Bogdanović, G. (2006). Synthesis and antitumour activity of new muricatacin and goniofufurone analogues. European Journal of Medicinal Chemistry, 41(10), 1217–1222. https://doi.org/10.1016/j.ejmech.2006.06.008
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