Helvetica Chimica Acta · 2007 · 15 citations · 6 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryAromatic PlantsHeterocyclic ChemistryTerpenoid BiosynthesisDiterpene BiosynthesisQuinone FormationSesquiterpene BiosynthesisTerpene CompoundsTerpenoid Cyclization Mechanisms
Abstract Two novel sesquiterpene dimers, compounds 1 and 2 , were isolated from the rhizome of Ligularia virgaurea , together with the six known sesquiterpenoids 3 – 8 . Their structures were established by physico‐chemical and spectroscopic methods, especially by means of 1D‐ and 2D‐NMR as well as HR‐MS analyses. A mechanism based on a classical Diels–Alder cyclization is proposed for the formation of the dimer 1 from the precursors 8 and the quinone form of 6 ( Scheme ).
6
Sesquiterpenoids from Ligularia virgaurea spp. oligocephala
Quan‐Xiang Wu, Ai‐Mei Yang, Yan‐Ping Shi · Tetrahedron · 2005 · 39 citations · Full text
Life Sciences, Biology, Mycology +2
benzofuranosesquiterpenes from Ligularia virgaurea
Zhong‐Jian Jia, Hongming Chen · Phytochemistry · 1991 · 35 citations
Francisco Yuste, F. Walls, Krzysztof Jankowski · The Journal of Organic Chemistry · 1976 · 31 citations