Synthesis of 4,5-seco-eudesman-type sesquiterpenes: 4,5-dioxo-10-epi-4,5-seco-?-eudesmane and 4,5-dioxo-10-epi-4,5-seco-?-eudesmanol
- 9 February 2005
- Vol. 17 (3) , 163-166
- https://doi.org/10.1002/chir.20127
Abstract
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This publication has 9 references indexed in Scilit:
- First Enantioselective Total Synthesis and Absolute Configurations of 4,5-Dioxo-seco-γ-eudesmol and 5β,11-Dihydroxyiphionan-4-one, Two Aglycones of Naturally Occurring Sesquiterpenes with New SkeletonsSynthesis, 2001
- First enantioselective total synthesis of glutinone and its C(7) and C(11) epimersTetrahedron: Asymmetry, 2001
- Sesquiterpenoids from Cyperus rotundusPhytochemistry, 1998
- Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens)Journal of Natural Products, 1997
- Two sesquiterpenoids, lucinone and glutinone, from Jasonia glutinosaPhytochemistry, 1995
- Sesquiterpene Xylosides from Iphiona mucronataJournal of Natural Products, 1990
- Sesquiterpene xylosides from Iphiona scabraPhytochemistry, 1987
- The structure and conformation of umbellifolide, a 4,5-secoeudesmane derivativeJournal of the Chemical Society, Perkin Transactions 1, 1983
- Generation and synthetic applications of 2-lithio-1,3-dithianesThe Journal of Organic Chemistry, 1975