Teurilene and thyrsiferyl 23-acetate, meso and remarkably cytotoxic compounds from the marine red alga laurencia obtusa (hudson) lamouroux
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (10), 1329-1332
- https://doi.org/10.1016/s0040-4039(00)94885-8
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Laurenyne, a new acetylene from Laurencia obtusa: crystal structure and absolute configurationTetrahedron Letters, 1980
- Obtusenyne, a new acetylenic nine-membrered cyclic ether fromTetrahedron Letters, 1979
- Obtusin, a unique bromine-containing polycyclic ketal from the red marine algaTetrahedron Letters, 1979
- X ray study of sesquiterpene constituents of the alga L obtusa leads to structure revisionTetrahedron Letters, 1979
- A new polyhalogenated sesquiterpene fromTetrahedron Letters, 1978
- Obtusadiol, a unique bromoditerpenoid from the marine red alga Laurencia ObtusaTetrahedron Letters, 1978
- The brasilenols, rearranged sesquiterpene alcohols isolated from the marine opisthobranch aplysia brasilianaTetrahedron, 1978
- 3β-Bromo-8-epicaparrapi oxide, the major metabolite of Laurencia obtusaPhytochemistry, 1976
- Evidence for the biogenesis of halogenated chamigrenes from the red alga laurencia obtusaTetrahedron Letters, 1976
- α- and β-snyderol; new bromo-monocyclic sesquiterpenes from the seaweedTetrahedron Letters, 1976