Synthesen DER Glycoside Von L-Nogalose und D-Evalose
- 1 March 1986
- journal article
- research article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 5 (1) , 67-76
- https://doi.org/10.1080/07328308608082643
Abstract
By stereospecific methylation at C-3 the lyxp-hexo-pyranoside-4-ulose is transformed into compound 1a. Mild acid cleavage of the isopropylidene groups and subsequent reduction proceeds to the 3-C-methyl manno-pyranoside 2a. This represents an efficient and fast access to D-evaloside or following permethylation to L-nogaloside.Keywords
This publication has 7 references indexed in Scilit:
- Eine Neue Einfache Synthese von L-VineloseJournal of Carbohydrate Chemistry, 1985
- Synthese des Tetradesoxydisaccharids D‐C der AureolsäurenEuropean Journal of Organic Chemistry, 1983
- Eine Neue Methode zur Synthese C - Verzweigter KohlenhydrateJournal of Carbohydrate Chemistry, 1983
- Synthesis of l-nogalose and its enantiomerCarbohydrate Research, 1981
- A stereospecific synthesis of evalose, a constituent of orthosomycin antibioticsCarbohydrate Research, 1981
- Structure of evernnomicin B.The Journal of Antibiotics, 1975
- Structure, absolute configuration, and chemistry of nogaloseThe Journal of Organic Chemistry, 1971