Chain Extension of Carbohydrates VI. Synthesis of the Two C-6 Epimers of the 6-Acetylamino-4,6-dideoxyheptopyranosiduronic Acid Present in Amipurimycin by Means of Stereocontrolled Ethynylation of Methyl 2,3-Di-O-benzyl-4-deoxy-α-D-xylo-hexodialdo-1,5-pyranoside
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/69/5/69_5_1347/_pdf
Reference11 articles.
1. Chain-Extension of Carbohydrates. 5. Synthesis of the C-Glycosyl Amino Acid Moiety of Miharamycins Involving Stereocontrolled Ethynylation of Methyl 2,3,4-Tri-O-benzyl-.alpha.-D-gluco-hexodialdo-1,5-pyranoside
2. Recent developments in the stereoselective synthesis of α-aminoacids
3. Isolation and characterization of a new nucleoside antibiotic, amipurimycin.
4. Streptomyces novoguineensis sp. nov., an amipurimycin producer, and antimicrobial activity of amipurimycin.
5. Structure of amipurimycin, a nucleoside antibiotic having a novel branched sugar moiety
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