Fullerene glycoconjugates: A general syn
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Arihiro Yashiro; Yoshihiro Nishida; Masatomi Ohno; Shoji Eguchi; Kazukiyo Kobaya
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Article
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1998
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Elsevier Science
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French
โ 239 KB
A general synthetic way to incorporate oligosaccharides into [60]fullerene via cycloadditon and deacetylation is presented. The cycloaddition reaction in refluxing chlorobenzene gave a mixture of two unseparable stereoisomers of N-~-glycopyranosyl [5,6]-azafulleroids in 13~28 % yields for per-O-acet