Syntheses of two enantiomers of eicos-(4E)-en-1-yn-3-ol, a bioactive component of the marine sponge Cribrochalina vasculum
- 1 April 1999
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 55 (15) , 4649-4654
- https://doi.org/10.1016/s0040-4020(99)00163-5
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Antitumor Activity and Stereochemistry of Acetylenic Alcohols from the Sponge Cribrochalina vasculumJournal of Natural Products, 1995
- Absolute stereochemistry of petroformynes, high molecular polyacetylenes from the marine sponge Petrosia ficiformisTetrahedron, 1994
- A Brief Synthesis of 3-Hydroxyeicos-4(E)-en-1-yne, a Component of Marine Sponge, Cribrochalina vasculumCollection of Czechoslovak Chemical Communications, 1993
- Further Bioactive Acetylenic Compounds from the Caribbean Sponge Cribrochalina vasculumJournal of Natural Products, 1992
- New acetylenic alcohols from the sponge Cribrochalina vasculumThe Journal of Organic Chemistry, 1990
- Enantiospecific Synthesis of Optically Pure Propargylic AlcoholsSynlett, 1990
- Carbohydrates as a practical source of chiral polyhydroxy acetylenesTetrahedron Letters, 1989
- An expeditious approach for the synthesis of optically active acetylenic alcoholsTetrahedron Letters, 1988
- The chemistry of D‐gluconic acid derivatives. Part 1: Synthesis of 3,4;5,6‐di‐O‐isopropylidene‐D‐glucitol and 2,3;4,5‐di‐O‐isopropylidene‐aldehydo‐D‐arabinose from D‐glucono‐1,5‐lactoneRecueil des Travaux Chimiques des Pays-Bas, 1987