Synthesen biologisch wichtiger Kohlenhydrate, 16. Stereoselektive Synthese der 3‐Dimethylamino‐2,3,6‐tridesoxy‐ ribo ‐hexose ( DL ‐Megosamin)
Author:
Affiliation:
1. Organisch‐Chemisches Institut der Universität Münster, Orléans‐Ring 23, D‐4400 Münster
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19791120233
Reference34 articles.
1. Arndt‐Eistert ‐Reaktionen in der Kohlenhydratchemie. — Synthesen biologisch wichtiger Kohlenhydrate, 15 Glycoside und Disaccharide aus Lactonen. — Lactonstrukturen und Ringdilatation
2. Synthesen biologisch wichtiger Kohlenhydrate, 13: Synthese des N ‐Acetyl‐ L ‐acosamins (3‐Acetylamino‐2,3,6‐tridesoxy‐ L ‐ arabino ‐hexose)
3. On physico-chemical interactions between daunomycin and nucleic acids
4. Synthesis and antitumor properties of new glycosides of daunomycinone and adriamycinone
5. Rhodosamin, eine neue Dimethylamino-desoxy-aldohexose
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4. Regio- and stereoselective conjugate addition of nitrogen nucleophiles to 2-alkenyl n-methylthiazolium iodides. synthesis of d-3-epi-daunosamine and some lincosamine analogues;Tetrahedron;1990-01
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