Biogenetic type synthesis of (±)-concinndiol and (±)-aplysin 20
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (3), 343-346
- https://doi.org/10.1016/s0040-4039(01)80813-3
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Syntheses of macrocyclic terpenoids by intramolecular cyclization III. model reactions for the synthesis of cembrene and thunbergol derivativesTetrahedron Letters, 1977
- Isoagatholactone, a diterpene of a new structural type from the sponge Spongia officinalisTetrahedron, 1974
- Stereoselective synthesis of trisubstituted olefinsTetrahedron Letters, 1973
- Marine natural products. Concinndiol, a bromo-diterpene alcohol from the red alga, Laurencia concinnaJournal of the Chemical Society, Chemical Communications, 1973
- Facile and specific conversion of allylic alcohols to allylic chlorides without rearrangementThe Journal of Organic Chemistry, 1971
- A Naturally-occurring Bromo-compound, Aplysin-20 from Aplysia kurodaiBulletin of the Chemical Society of Japan, 1971