Studies on the syntheses of sesquiterpene lactones. 11. The syntheses of 3-epizaluzanin C, zaluzanin C, zaluzanin D, and related compounds 3.alpha.-hydroxyguaia-1(10),4(15),11(13)-trieno-12,6.alpha.-lactone and 3.alpha.-hydroxyguaia-4(15),9,11(13)-trieno-12,6.alpha.-lactone
- 1 April 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (8) , 1952-1960
- https://doi.org/10.1021/jo00269a039
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Syntheses of arborescin, 1,10-epiarborescin, and (11S)-guaia-3,10(14)-dieno-13,6.alpha.-lactone, the key intermediate in Greene and Crabbe's estafiatin synthesis, and the stereochemical assignment of arborescinThe Journal of Organic Chemistry, 1982
- Stereocontrolled total synthesis of an .alpha.-methylene guaianolide in the 4,5-epoxyosmitopsin familyJournal of the American Chemical Society, 1980
- A Bitter Principle of Pertya robusta (MAXIM.) BEAUV. : Glucozaluzanin CYAKUGAKU ZASSHI, 1980
- Biomimetic cyclization of gallicin to form guaianolidesTetrahedron, 1980
- Mono- and sesquiterpenoids from Wiesnerella denudataPhytochemistry, 1980
- Stereoselective synthesis of (-)-estafiatinThe Journal of Organic Chemistry, 1979
- Sesquiterpene lactones of Conocephalum conicumPhytochemistry, 1979
- Anticancer sesquiterpene lactones of Michelia compressa (magnoliaceae)Phytochemistry, 1978
- A new type of germacranolide from Vernonia speciesPhytochemistry, 1978
- Biological activities of sesquiterpene lactonesPhytochemistry, 1976