Synthesis of some further C-3 branched 3-amino-2,3,6-trideoxysugars, related to daunosamine, as potential components for structurally modified anthracyclines-Reference-Cited by-同舟云学术

Synthesis of some further C-3 branched 3-amino-2,3,6-trideoxysugars, related to daunosamine, as potential components for structurally modified anthracyclines

Published:1992-12 Issue: Volume:237 Page:145-160
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Santoyo González Francisco,Vargas Berenguel Antonio,Hernández Mateo Fernando,García Mendoza Pilar,Baer Hans H

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference23 articles.

1. Synthesis and Reactivity of Sugars with Two Branches at C-3

2. Synthesis and biological activity of (S)-2′-fluorodaunorubicin

3. Synthesis of 3-amino-2,3,6-trideoxy-2-fluoro-l-talose and -d-allose [(R)-2-fluoro-l-daunosamine and (R)-2-fluoro-d-ristosamine]

4. Synthesis and biological activity of (R)-2′-fluorocarminomycin

5. Synthesis of 3-C-carbamoyl-3-C-cyano-3-deoxyhexopyranosides by cyclization of dialdehydes with cyanoacetamide

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