The use of selective lactonisation to achieve chemodifferentiation of two carboxylic acid functions. A novel entry into the elemanolide sesquiterpenes.
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (4) , 473-474
- https://doi.org/10.1016/s0040-4039(00)61914-7
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Studies on the syntheses of sesquiterpene lactones. 8. Syntheses of saussurea lactone, 8-deoxymelitensin, and 11,12-dehydro-8-deoxymelitensin via a novel fragmentation reactionThe Journal of Organic Chemistry, 1983
- The control of regiochemistry in the alkylation of indanone derivativesJournal of the Chemical Society, Chemical Communications, 1982
- Total synthesis of (.+-.)-vernolepinJournal of the American Chemical Society, 1978
- Synthesis of sesquiterpene antitumor lactones. 2. A new stereocontrolled total synthesis of (.+-.)-vernolepinJournal of the American Chemical Society, 1978
- The total synthesis of dl-vernolepin and dl-vernomeninJournal of the American Chemical Society, 1977
- Sesquiterpene lactones: total synthesis of (.+-.)-vernolepin and (.+-.)-vernomeninJournal of the American Chemical Society, 1977