Studies on the dehydrative cyclization of epimeric 4-(L-xylo and L-lyxo-tetritol-1-yl)-2-phenyl-2H-1,2,3-triazoles. Circular dichroism and NMR assignment of the formed anomericC-nucleoside L-threofuranosyl triazole analogs-Reference-Cited by-同舟云学术

Studies on the dehydrative cyclization of epimeric 4-(L-xylo and L-lyxo-tetritol-1-yl)-2-phenyl-2H-1,2,3-triazoles. Circular dichroism and NMR assignment of the formed anomericC-nucleoside L-threofuranosyl triazole analogs

Published:2004 Issue:5 Volume:16 Page:331-335
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Sallam Mohammed A.E.,Louis Farida F.

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference16 articles.

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2. The carbohydrates: chemistry and biochemistry, vol. IIA. New York: Academic Press; 1970. p 139-211.

3. C-glycoside synthesis. Ann Arbor: CRC Press; 1995. p 303-366.

4. 3-β-d-erythrofuranosyl-1-phenylpyrazolo[3,4-b]quinoxaline, a new C-nucleoside analog

5. Studies on 3-epimeric 2-hexulose phenylosazones. structure and anomeric configuration of the 3,6-anhydro-osazone derivatives obtained from d-arabino- and d-ribo-2-hexulose phenylosazone

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