Abstract
α-D-Arabinofuranosyl-(1→5)-[α-D-arabinofuranosyl-(1→3)]-α-D-arabinofuranosyl-(1→5)-Darabinofuranose (6) present in motif B of the Mycobacterium tuberculosis cell wall was regio- and stereospecifically synthesized by trichloroacetimidate method. The strategy greatly simplified the procedure for synthesizing 6.
Keywords: Carbohydrate, synthesis, arabinofuranose, oligosaccharide, glycosylation, trichloroacetimidate
Letters in Organic Chemistry
Title: Synthesis of a Tetrasaccharide Present in Motif B of the Mycobacterium tuberculosis Cell Wall
Volume: 2 Issue: 8
Author(s): Linsen Heng, Xiangdong Mei, Zhe Yao and Jun Ning
Affiliation:
Keywords: Carbohydrate, synthesis, arabinofuranose, oligosaccharide, glycosylation, trichloroacetimidate
Abstract: α-D-Arabinofuranosyl-(1→5)-[α-D-arabinofuranosyl-(1→3)]-α-D-arabinofuranosyl-(1→5)-Darabinofuranose (6) present in motif B of the Mycobacterium tuberculosis cell wall was regio- and stereospecifically synthesized by trichloroacetimidate method. The strategy greatly simplified the procedure for synthesizing 6.
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Cite this article as:
Heng Linsen, Mei Xiangdong, Yao Zhe and Ning Jun, Synthesis of a Tetrasaccharide Present in Motif B of the Mycobacterium tuberculosis Cell Wall, Letters in Organic Chemistry 2005; 2 (8) . https://dx.doi.org/10.2174/157017805774717562
DOI https://dx.doi.org/10.2174/157017805774717562 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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