18918-36-0Relevant articles and documents
Synthesis of aryl α-O-L-rhamnopyranoside by two-step reaction in one pot
Liu, Nianping,Tian, Xiangguang,Ding, Zekun,Zhou, Yongda,Zhang, Wan,Wang, Qingbing,Zhang, Yi,Gu, Yijun,Zhang, Jianbo
, p. 220 - 234 (2017/11/10)
The title compounds were conveniently synthesized by a phase transfer catalyzed approach in two steps and one pot using the rhamnopyranosyl chloride as key intermediate. The twostep one-pot procedure is more convenient and environmentally friendly, compared to the published synthetic routes. Besides, the structure-reactivity relationship and the plausible mechanism for this base-catalyzed glycosylation were discussed bymeans of the Hammett equation.
Using biological performance similarity to inform disaccharide library design
Tanikawa, Tetsuya,Fridman, Micha,Zhu, Wenjiang,Faulk, Brian,Joseph, Isaac C.,et al.
supporting information; experimental part, p. 5075 - 5083 (2009/09/30)
Designing better small-molecule discovery libraries requires having methods to assess the consequences of different synthesis decisions on the biological performance of resulting library members. Since we are particularly interested in how stereochemistry
ANTIBODIES FOR THE DETECTION OF BACILLUS ANTHRACIS AND VACCINE AGAINST B. ANTHRACIS INFECTIONS
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Page/Page column 20, (2008/06/13)
35 Abstract The present invention relates to conjugates of oligosaccharides of formula 1, wherein R is a linker to a carrier protein and optionally comprises up to three further saccharides, 5 and which are useful for vaccination, methods of synthesis of