Glycosylimidate, 35 Synthese eines Cerebrosids mit (4E,8E)-Sphingadienin-Struktur ausTetragonia tetragonoides mit antiulcerogener Aktivität
- 14 July 1988
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1988 (7) , 669-674
- https://doi.org/10.1002/jlac.198819880709
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Glycolipids of Marine InvertebratesPublished by Elsevier ,1987
- Tumor-associated glycolipid antigens, their metabolism and organizationChemistry and Physics of Lipids, 1986
- Neue Methoden zur Glycosid- und Oligosaccharidsynthese – gibt es Alternativen zur Koenigs-Knorr-Methode?Angewandte Chemie, 1986
- New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]Angewandte Chemie International Edition in English, 1986
- Space Science, Space Technology and the Space StationScientific American, 1986
- A hypothesis on the biological role of ABH, lewis and P blood group determinant structures in glycosphingolipids and glycoproteinsGlycoconjugate Journal, 1986
- Demonstration by monoclonal antibodies that carbohydrate structures of glycoproteins and glycolipids are onco-developmental antigensNature, 1985
- Tumor-Associated Carbohydrate AntigensAnnual Review of Immunology, 1984
- The principles of Tetragonia tetragonoides having anti-ulcerogenic activity. II. Isolation and structure of cerebrosides.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- The stereochemistry of α-oxidation of fatty acids in plants: the configuration of biosynthetic long-chain 2-hydroxy acidsBiochemical Journal, 1971