Syntheses of All Four Possible Diastereomers of Etoposide and Its Aminoglycosidic Analogues via Optical Resolution of (±) -Podophyllotoxin by Glycosidation with D- and L-Sugars-Reference-Cited by-同舟云学术

Syntheses of All Four Possible Diastereomers of Etoposide and Its Aminoglycosidic Analogues via Optical Resolution of (±) -Podophyllotoxin by Glycosidation with D- and L-Sugars

Published:1987-05-05 Issue:5 Volume:16 Page:799-802
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Saito Hitoshi,Nishimura Yoshio,Kondo Shinichi,Umezawa Hamao

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference7 articles.

1. VP16-213 (Etoposide)

2. VM26: Phase I and II studies

3. Studies on lignan lactone antitumor agents. I Synthesis of aminoglycosidic lignan variants related to podophyllotoxin.

4. Studies on lignan lactone antitumor agents. II Synthesis of N-alkylamino- and 2,6-dideoxy-2-aminoglycosidic lignan variants related to podophyllotoxin.

5. A stereocontrolled synthesis of antineoplastic podophyllum lignans

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