Stereocontrolled total synthesis of an .alpha.-methylene guaianolide in the 4,5-epoxyosmitopsin family
- 1 December 1980
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 102 (25) , 7498-7505
- https://doi.org/10.1021/ja00545a017
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Stereoselective synthesis of (-)-estafiatinThe Journal of Organic Chemistry, 1979
- Sesquiterpene lactones of eupatorium anomalum and eupatorium mohriiPhytochemistry, 1979
- Sesquiterpene lactones of Conocephalum conicumPhytochemistry, 1979
- Anticancer sesquiterpene lactones of Michelia compressa (magnoliaceae)Phytochemistry, 1978
- Cis-Kolaveninsäure und weitere inhaltsstoffe aus vertretern der tribus eupatorieaePhytochemistry, 1978
- New sesquiterpene lactones from Inula speciesPhytochemistry, 1978
- Chemical transformations of abundant natural products. 3. Modifications of eremanthin leading to other naturally occurring guaianolidesThe Journal of Organic Chemistry, 1977
- Antitumor agents. 25. Synthesis and antitumor activity of uracil and thymine .alpha.-methylene-.gamma.-lactones and related derivativesJournal of Medicinal Chemistry, 1977
- Biological activities of sesquiterpene lactonesPhytochemistry, 1976
- Estafiatin, a new sesquiterpene lactone isolated from Artemisia mexicana (Willd)Tetrahedron, 1963