Abspaltung von Acyl-Schutzgruppen bei alkaliempfindlichen Glucosiden. - Synthese von Podophyllotoxin-?-D-glucosid. 20. Mitteilung �ber mitosehemmende Naturstoffe [1]-Reference-Cited by-同舟云学术

Abspaltung von Acyl-Schutzgruppen bei alkaliempfindlichen Glucosiden. - Synthese von Podophyllotoxin-?-D-glucosid. 20. Mitteilung �ber mitosehemmende Naturstoffe [1]

Published:1968-01-31 Issue:1 Volume:51 Page:163-168
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Kuhn M.,Von Wartburg A.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference16 articles.

1. Podophyllum- Lignane: Struktur und Absolutkonfiguration von Podorhizol-?-D-glucosid ( = Lignan F). 19. Mitt. �ber mitosehemmende Naturstoffe [1]

2. Die Isolierung von Podophyllotoxin-glucosid aus dem indischen Podophyllum emodiWall. 2. Mitteilung über mitosehemmende Naturstoffe

3. Lignanglucoside ausPodophyllum peltatum L. 7. Mitteilung über mitosehemmende Naturstoffe

4. Zur Struktur des Sikkmotoxins II. Partialsynthese der 6,7-Dimethoxy-Analogen von Podophyllotoxin, Epi-, Neo- und Desoxy-podophyllotoxin 17. Mitteilung über mitosehemmende Naturstoffe [1]

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