Selective modification of mono-altro-β-cyclodextrin: dependence of O-sulfonylation position on the shape of sulfonylating reactant
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
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2. Biomimetic Reactions Catalyzed by Cyclodextrins and Their Derivatives
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4. Guest-induced conformational change in a flexible host: mono-altro-β-cyclodextrin
5. Restriction of guest rotation based on the distortion of a cyclodextrin cavity
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1. The effect of urea moiety in amino acid binding by β-cyclodextrin derivatives: A 1000-fold increase in efficacy comparing to native β-cyclodextrin;Carbohydrate Polymers;2017-05
2. Free-energy landscapes of the coupled conformational transition and inclusion processes of altro-cyclodextrins;Molecular Simulation;2017-03-09
3. Selective Secondary Face Modification of Cyclodextrins by Mechanosynthesis;The Journal of Organic Chemistry;2015-06-08
4. Hetero-bifunctionalization of the secondary face of β-cyclodextrin: selective 3G-sulfonylation and subsequent 2G,3G-epoxidation of 3A-azido-3A-deoxy-altro-β-cyclodextrin;Tetrahedron Letters;2006-09
5. Selective mono-O-sulfonylation of A,B-di-altro- β-cyclodextrin by utilizing restricted orientation of a guest-type sulfonylating reactant in the elliptically distorted cavity: the 2A-O- and 3G-O-2-naphthalenesulfonates as a versatile scaffold to prepare artificial enzymes with controlling substrate orientation;Tetrahedron Letters;2004-09
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