Reaktionen enolischer Zuckerderivate, XI. Umsetzung von Methyl-3,4-anhydro-6-desoxy-α-L-arabino-hex-5-enopyranosid und -β-L-arabino-hex-5-enopyranosid mit Nucleophilen-Reference-Cited by-同舟云学术

Reaktionen enolischer Zuckerderivate, XI. Umsetzung von Methyl-3,4-anhydro-6-desoxy-α-L-arabino-hex-5-enopyranosid und -β-L-arabino-hex-5-enopyranosid mit Nucleophilen

Published:1976-02-03 Issue:1 Volume:1976 Page:89-96
ISSN:0075-4617
Container-title:Justus Liebigs Annalen der Chemie
language:de
Short-container-title:Justus Liebigs Ann. Chem.

Author:

Brockhaus Manfred,Gorath Werner,Lehmann Jochen

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,General Medicine

Reference10 articles.

1. Reaktionen enolischer Zuckerderivate, X1) Allylaktivierung in 4- und 3-O-Tosylestern von Hex-5-enopyranosiden

2. Synthesis and Chemistry of 4-Amino-4,6-dideoxy Sugars. II. Glucose1

3. Über Steroide und Sexualhormone. 160. Mitteilung. 2α, 3α- und 2β, 3β-Oxido-chlolestane; Konfiguration der 2-Oxy-cholestane

4. Notes - Osmium Tetroxide-Catalyzed Periodate Oxidation of Olefinic Bonds

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