An efficient synthesis of selectively functionalized D-rhamnose derivatives
M Zunk, MJ Kiefel
Index: Zunk, Matthew; Kiefel, Milton J. Tetrahedron Letters, 2011 , vol. 52, # 12 p. 1296 - 1299
Full Text: HTML
Citation Number: 7
Abstract
d-Rhamnose is an important component of bacterial lipopolysaccharides. This paper describes a short and highly efficient synthesis of d-rhamnose from d-mannose. The synthesis of selectively C-4 modified d-rhamnosides and 6-deoxy-d-talosides as potential building blocks for complex oligosaccharide synthesis is also discussed.
Related Articles:
[Li, Tiehai; Wen, Liuqing; Williams, Adriel; Wu, Baolin; Li, Lei; Qu, Jingyao; Meisner, Jeffrey; Xiao, Zhongying; Fang, Junqiang; Wang, Peng George Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 3 p. 1139 - 1147]
Synthesis of β??(1→ 2)??Linked Oligomannosides
[Polakova, Monika; Roslund, Mattias U.; Ekholm, Filip S.; Saloranta, Tiina; Leino, Reko European Journal of Organic Chemistry, 2009 , # 6 p. 870 - 888]
[Bashyal, Bharat P.; Fleet, George W. J.; Gough, Max J.; Smith, Paul W. Tetrahedron, 1987 , vol. 43, # 13 p. 3083 - 3094]
The synthesis of the heptose region of the gram-negative bacterial core oligosaccharides
[Dziewiszek, Krzysztof; Banaszek, Anna; Zamojski, Aleksander Tetrahedron Letters, 1987 , vol. 28, # 14 p. 1569 - 1572]