Organic Letters · 2012 · 42 citations · 21 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsHeterocyclic ChemistryHeterocyclic CompoundsMolecular SimilarityNatural Product Drug DiscoveryStructure-activity Relationship AnalysisTerpenoid BiosynthesisMedicinal HeterocyclesSingle-crystal DiffractionSingle-crystal X-ray DiffractionTriterpene Biosynthesis
A pair of new triterpenoid epimers, kadcoccitones A (1) and B (2), together with a new biogenetically related compound kadcoccitone C (3), were isolated from Kadsura coccinea. The epimers featured an unprecedented carbon skeleton with a 6/6/5/5-fused tetracyclic ring system unit and a C(9) side chain. Their structures were determined by spectroscopic data, ECD calculation, and single-crystal X-ray diffraction. Compounds 1 and 3 showed anti-HIV-1 activity with an EC(50) value of 47.91 and 32.66 μg/mL, respectively.
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Diastereoselective Total Synthesis of (±)‐Schindilactone A
Qing Xiao, Weiwu Ren, Zhixing Chen et al. · Angewandte Chemie International Edition · 2011 · 164 citations
Schinalactone A, a New Cytotoxic Triterpenoid from <i>Schisandra sphenanthera</i>
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