Organic Letters · 2013 · 43 citations · 19 references
New Indole AlkaloidsMedicinal ChemistryCommon Cleavamine-type IntermediateNatural SciencesMedicineDiversity-oriented SynthesisOrganic ChemistryStereoselective SynthesisHeterocycle ChemistryNovel AlkaloidsPharmacologyIboga PrecursorEnantioselective SynthesisDrug DiscoveryNatural Product Synthesis
Two new indole alkaloids, voatinggine (1) and tabertinggine (2), which are characterized by previously unencountered natural product skeletons, were isolated from a Malayan Tabernaemontana species. The structures and absolute configuration of these alkaloids were determined using NMR and MS analysis, and X-ray diffraction analysis. A possible biogenetic pathway to these novel alkaloids from an iboga precursor, and via a common cleavamine-type intermediate, is presented.
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The Total Synthesis of Iboga Alkaloids<sup>1</sup>
G. Büchi, David L. Coffen, Karoly Kocsis et al. · Journal of the American Chemical Society · 1966 · 97 citations
Rhazinilam–Leuconolam–Leuconoxine Alkaloids from <i>Leuconotis griffithii</i>
Chew‐Yan Gan, Yun‐Yee Low, Noel F. Thomas et al. · Journal of Natural Products · 2013 · 69 citations