Enantioselective Syntheses and Absolute Configurations of Viridiene and Aucantene, Two Constitutents of Algae Pheromone Bouquets
- 13 November 1985
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 68 (7), 2062-2073
- https://doi.org/10.1002/hlca.19850680731
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Viridiene ? the male gamete attractant of the brown alga Syringoderma phinneyi ? has 3R,4S-configurationThe Science of Nature, 1985
- Complexation gas chromatographyThe Science of Nature, 1984
- Viridiene, the sexual pheromone of Syringoderma (Phaeophyceae)The Science of Nature, 1982
- Signalstoffe und ihre Reception im Sexualcyclus mariner BraunalgenAngewandte Chemie, 1982
- Signal Substances and their Reception in the Sexual Cycle of Marine Brown AlgaeAngewandte Chemie International Edition in English, 1982
- Enzymes in organic synthesis. 24. Preparations of enantiomerically pure chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of monocyclic meso diolsJournal of the American Chemical Society, 1982
- Identification of a sexual hormone and related substances in the marine brown alga DesmarestiaThe Science of Nature, 1982
- Separation of enantiomers by high-performance liquid chromatography on triacetylcelluloseJournal of Chromatography A, 1980
- Multifidene and aucantene, C11 hydrocarbons in the male-attracting essential oil from the gynogametes of Cutleria multifida (Phaeophyta)Journal of the American Chemical Society, 1974
- A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′)Tetrahedron Letters, 1972