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Showing papers by "Eberhardt Herdtweck published in 2017"


Journal ArticleDOI
TL;DR: It is indicated that the promising biological activity can be retained by structurally simpler natural product analogues, which are accessible by a straightforward synthetic route.
Abstract: Neurotrophic natural products hold potential as privileged structures for the development of therapeutic agents against neurodegeneration. However, only a few studies have been conducted to investigate a common pharmacophoric motif and structure–activity relationships (SARs). Here, an investigation of structurally more simple analogues of neurotrophic sesquiterpenes of the illicium family is presented. A concise synthetic route enables preparation of the carbon framework of (±)-Merrilactone A and (±)-Anislactone A/B on a gram scale. This has allowed access to a series of structural analogues by modification of the core structure, including variation of oxidation levels and alteration of functional groups. In total, 15 derivatives of the natural products have been synthesized and tested for their neurite outgrowth activities. Our studies indicate that the promising biological activity can be retained by structurally simpler natural product analogues, which are accessible by a straightforward synthetic route.

17 citations


Journal ArticleDOI
TL;DR: A new metallic radical cation salt κ•(BETS) 2 Co 0.13 Mn 0.87 [N(CN) 2 ] 3, where BETS is bis(ethylenedithio)tetraselenafulvalene, C 10 S 4 Se 4 H 8, has been synthesized as discussed by the authors.

3 citations