Organic Letters · 2017 · 59 citations · 22 references
Natural SciencesBotanyChemistryDrug DiscoveryOrganic ChemistryPlant BiochemistryHeterocyclic ChemistryHeterocyclic CompoundsMedicinal PlantsTerpenoid BiosynthesisBiosynthetic Pathway AnalysisDiterpene BiosynthesisMonoterpene BiosynthesisSingle-crystal DiffractionSingle-crystal X-ray Diffraction
A novel diterpenoid with an unprecedented carbon skeleton, rhodomollanol A (1), and a new grayanane diterpenoid, rhodomollein XXXI (2), were isolated from the leaves of Rhododendron molle. Their structures were elucidated using comprehensive spectroscopic methods and single-crystal X-ray diffraction. Compound 1 possesses a unique cis/trans/trans/cis/cis-fused 3/5/7/5/5/5 hexacyclic ring system featuring a rare 7-oxabicyclo[4.2.1]nonane core decorated with three cyclopentane units. The plausible biosynthetic pathway for 1 was proposed. Compound 1 exhibited moderate PTP1B inhibitory activity.
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Total Synthesis of (-)-Grayanotoxin III
Toshiyuki Kan, Seijiro Hosokawa, Shinji Nara et al. · The Journal of Organic Chemistry · 1994 · 121 citations
Grayanoid diterpene insect antifeedants and insecticides from Rhododendron molle
James A. Klocke, HU Mei‐ying, Shin‐Foon Chiu et al. · Phytochemistry · 1991 · 105 citations
Antinociceptive Grayanoids from the Roots of <i>Rhododendron molle</i>
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