Total synthesis of (±) stoechospermol
- 19 September 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (38) , 7031-7032
- https://doi.org/10.1016/0040-4039(94)88217-7
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Non photochemical synthesis of condensed cyclobutenes. Syntheses of the cis-anti-cis-tricyclo [5.3.0.02,6] decane skeleton.Tetrahedron Letters, 1993
- Total synthesis of spatol and other spatane diterpenesJournal of the American Chemical Society, 1991
- Asymmetric total synthesis of stoechospermol using intramolecular (2+2) photocycloaddition reactionTetrahedron Letters, 1985
- Stereocontrol of Michael hydride reduction by a remote hydroxyl group. A strategy for stereorational total synthesis of spatane diterpenesJournal of the American Chemical Society, 1984
- Spatane diterpenoids from the tropical marine algae Spatoglossum schmittii and Spatoglossum howleii (Dictyotaceae)The Journal of Organic Chemistry, 1983
- Spatane diterpenoids from the tropical marine alga Stoechospermum marginatum (Dictyotaceae)The Journal of Organic Chemistry, 1981
- Total stereospecific synthesis ofTetrahedron Letters, 1980
- Isolation and structure of spatol, a potent inhibitor of cell replication from the brown seaweed Spatoglossum schmittiiJournal of the American Chemical Society, 1980
- Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compoundsTetrahedron Letters, 1975
- The Wittig Reaction Using Methylsulfinyl Carbanion-Dimethyl Sulfoxide 1The Journal of Organic Chemistry, 1963