Stereostructures of two biologically active sesquiterpene lactones from Inula racemosa
- 31 December 1989
- journal article
- Published by Elsevier BV in Phytochemistry
- Vol. 28 (8), 2093-2096
- https://doi.org/10.1016/s0031-9422(00)97926-3
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Epoxy alantolides: Isoinunal—a new potent plant growth regulator from Inula racemosaPhytochemistry, 1988
- Absinthifolide a sesquiterpene glycoside from bahia absinthifolia var. absinthifoliaPhytochemistry, 1987
- Stereostructures of inunal and isoalloalantolactone, two biologically active sesquiterpene lactones from Inula racemosaPhytochemistry, 1985
- Regulation of nitrate reductase activity in higher plantsPhytochemistry, 1980
- Biogenetically patterned transformation of eudesmanolide to eremophilanolide. IV. Conversion of alantolactone to several furanoeremophilane derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1977
- Biogenetically patterned transformation of eudesmanolide to eremophilanolide. II. Structures of minor products obtained by acid treatment of 5.ALPHA., 6.ALPHA.-epoxy-eudesman-8.BETA., 12-olide.CHEMICAL & PHARMACEUTICAL BULLETIN, 1976
- A highly stereoselective total synthesis of (±)-isoalantolactoneTetrahedron, 1974
- HORMONAL REGULATION OF NITRATE REDUCTASE ACTIVITY IN LEAVESNew Phytologist, 1970
- Light and Hormones: Interchangeability in the Induction of Nitrate ReductaseScience, 1969
- The Structure of AlantolactoneJournal of the American Chemical Society, 1957