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

Literature Information

Publication Date 2005-05-18
DOI 10.1039/B502573G
Impact Factor 6.222
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Abstract

The A-ring of 2A,2B-O,O-di(mesitylenesulfonyl)-β-cyclodextrin was converted to 2A,3A-epoxymannoside without affecting the other sulfonylated residue, which affords the first approach to hetero-bifunctionalization at the secondary hydroxyl side of cyclodextrins.

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