Abstract
The importance of the sesquiterpene lactone thapsigargin as a tool for studying Ca2+ homeostasis has created a need for structure-activity relationship studies and consequently for procedures for selective transformations of the functional groups in the molecule. Methods for the selective inversion of configuration at C-3 and C-8, selective acetylation, and selective cleavage of the ester groups at 0-3, 0-8 and 0-10 are presented.
Originalsprog | Udefineret/Ukendt |
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Tidsskrift | Acta Chemica Scandinavica. Supplementum |
Vol/bind | 48 |
Udgave nummer | 4 |
Sider (fra-til) | 340-346 |
Antal sider | 7 |
ISSN | 0065-1133 |
Status | Udgivet - 1994 |
Emneord
- ca2+ transport atpases reticulum ca-2+-atpase thapsia-garganica tumor promoter high-affinity