首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Selective functionalization of p-cyclodextrin:efficient conversions of 2,3-alloepoxypyranosides to 2,3-mannoepithiopyranosides
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Selective functionalization of p-cyclodextrin:efficient conversions of 2,3-alloepoxypyranosides to 2,3-mannoepithiopyranosides

机译:对-环糊精的选择性功能化:2,3-alloepoxypyranosides高效转化为2,3-mannoepithiopyranosides

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摘要

A two-step one-pot method was established to efficiently convert up to three 2,3-alloepoxypyranoside residues to the 2,3-mannoepithiopyranosides within the P-cyclodextrin belts.Many artificial enzymes have been made by the func-tionalizations of cyclodextrins(CDs)whose cavities afford substrate-binding sites.Mono-to poly-function-alizations including homo and hetero ones on the primary hydroxyl sides have been extensively studied.
机译:建立了两步一锅法,可将P-环糊精带中的多达3个2,3-alloepoxypyranyside残基有效地转化为2,3-mannoepithiopyranosides。许多人工酶是通过环糊精的功能化制备的(其空腔提供底物结合位点的CD。已经广泛研究了伯羟基上的均一和多官能化,包括均相和杂合。

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