The first hetero-bifunctionalization of the secondary face of β-cyclodextrin:: selective and efficient conversion of the A-ring of a 2A,2B-disulfonate to 2A,3A-epoxymannoside
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Fukudome, M
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Sugimoto, Y
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Nagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, JapanNagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, Japan
Sugimoto, Y
[1
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Yuan, DQ
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Nagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, JapanNagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, Japan
Yuan, DQ
[1
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Fujita, K
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Nagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, JapanNagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, Japan
Fujita, K
[1
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[1] Nagasaki Univ, Dept Mol Med Sci, Grad Sch Biomed Sci, Nagasaki, Japan
The A-ring of 2(A),2(B)-O,O-di(mesitylenesulfonyl)-beta-cyclodextrin was converted to 2(A),3(A)-epoxymannoside without affecting the other sulfonylated residue, which affords the first approach to hetero-bifunctionalization at the secondary hydroxyl side of cyclodextrins.