Preparation of 4-O-acetyl-1,5-anhydro-2,3,6-trideoxy-3-trifluoroacetamido-l- lyxo-hex-1-enitol, a key intermediate in synthesis of daunosamine glycosides-Reference-Cited by-同舟云学术

Preparation of 4-O-acetyl-1,5-anhydro-2,3,6-trideoxy-3-trifluoroacetamido-l- lyxo-hex-1-enitol, a key intermediate in synthesis of daunosamine glycosides

Published:1989-04 Issue:1 Volume:187 Page:145-148
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Horton Derek,Priebe Waldemar,Sznaidman Marcos

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference9 articles.

1. D. Horton and W. Priebe, U.S. Patent 4 562 177, Dec. 31, 1985

2. Synthesis and antitumor activity of sugar-ring hydroxyl analogs of daunorubicin

3. 7-O-(3-Amino-2,3,6-trideoxy-α-D-ribo-hexopyranosyl)daunomycinone, a configurational analog of daunorubicin

4. Synthesis of antitumor-active (7S,9S)-4-demethoxy-7-O-(2,6-dideoxy-2-iodo-α-l-mannopyranosyl)adriamycinone: Preparative resolution of a racemic anthracyclinone by alkoxyhalogenation of a glycal

5. Synthesis and antitumor activity of 2′-bromo- and 2′-chloro-3′-acetoxy-3′-deaminodaunorubicin analogs

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3. Formation and Reactions of Glycal Derivatives;Glycoscience: Chemistry and Chemical Biology I–III;2001

4. Synthesis and antitumor activity of anthracycline disaccharide glycosides containing daunosamine.;The Journal of Antibiotics;1993

5. One step C-acylation of glycals and 2-deoxy-hexopyranoses at C-2;Tetrahedron Letters;1992-12