Abstract
Four new securinega alkaloids, flueggeacosines D–F and securingine J, have been discovered from Flueggea suffruticosa. Flueggeacosines D and E possess dimeric frameworks incorporating a benzoquinolizidine motif derived from allosecurinine backbone. A concise synthetic strategy combining TBADT-catalyzed radical hydroacylation and Mo(CO)₆-mediated reductive rearrangement enabled efficient access to these complex alkaloids. Our synthetic approach also realized a synthesis-based natural product anticipation that predicted and confirmed the existence of flueggeacosine F and securingine J in F. suffruticosa. Furthermore, oxidative rearrangements of flueggeacosine A furnished flueggeacosines D and F, supporting a plausible biosynthetic linkage. These findings establish a unified route to oxidized dimeric securinega alkaloids and demonstrate the synergy of synthesis and biosynthetic reasoning in natural product discovery.
Supplementary materials
Title
Supporting Information
Description
Isolation details, experimental procedures and physical data for newly synthesized compounds, computational analysis, and copies of NMR spectra
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