Organic Letters · 2019 · 11 citations · 23 references
Natural SciencesBiochemistryChemistryBiogeochemistryMetabolismOrganic ChemistryBioinorganic ChemistryChiral ChromatographyMacrocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisMacrolide GlycosidesStereoselective Synthesis
Luteolide is a 10-membered aliphatic macrolactone, (4 R,8 S,9 S)-4,8-dimethylundecan-9-olide ((-) -17), released by the femoral gland of males of the mantellid frog Gephyromantis luteus. Its structure was established using NMR, MS, and chiral GC and confirmed by stereoselective synthesis of different stereoisomers. Among the approximately 20 current macrolides known from the Mantellidae, luteolide is the first example of a volatile macrolide furnishing three stereogenic centers and an ethyl side chain.
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Herbert C. Brown, K. S. BHAT · Journal of the American Chemical Society · 1986 · 380 citations
Natural Sciences, Chemistry, Natural Product Biosynthesis +5
Decanolides, 10-membered lactones of natural origin
Gerald Dräger, Andreas Kirschning, Ralf Thiericke et al. · Natural Product Reports · 1996 · 115 citations