relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides from marine sponge diacarnus megaspinorhabdosa

relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides from marine sponge diacarnus megaspinorhabdosa

;Fan Yang;Yike Zou;Ru-Ping Wang;Mark T. Hamann;Hong-Jun Zhang;Wei-Hua Jiao;Bing-Nan Han;Shao-Jiang Song;Hou-Wen Lin
jixie gongcheng xuebao/journal of mechanical engineering 2014 Vol. 12 pp. 4399-4416
254
yang2014marinerelative

Abstract

Five new norditerpene endoperoxides, named diacarperoxides H–L (1–5), and a new norditerpene diol, called diacardiol B (6), were isolated from the South China Sea sponge, Diacarnus megaspinorhabdosa. Their structures, including conformations and absolute configurations, were determined by using spectroscopic analyses, computational approaches and chemical degradation. Diacarperoxides H–J (1–3) showed some interesting stereochemical issues, as well as antimalarial activity.

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