Synthetic route for selective modification of the secondary hydroxyl face of cyclodextrins
Author:
Publisher
Informa UK Limited
Subject
General Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10610279308029815
Reference15 articles.
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3. Separation of enantiomers by clathrate formation
4. A new cycloglucohexaose derivative the chemical synthesis of Cyclo{→3-[β-D-Glcp-(1→3)-]5-D-Glcp(1→)}
5. Cyclodextrin-based enzyme models. Part 1. Synthesis of a tosylate and an epoxide derived from heptakis(6-O-tert-butyldimethylsilyl)-β-cyclodextrin and their characterization using 2D NMR techniques. An improved route to cyclodextrins functionalized on the secondary face
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1. Facile synthesis of per(6-O-tert-butyldimethylsilyl)-α-, β-, and γ-cyclodextrin as protected intermediates for the functionalization of the secondary face of the macrocycles;Nature Protocols;2021-01-15
2. Selectively functionalized cyclodextrins and their metal complexes;Chemical Society Reviews;2009
3. A facile sulfonylation method enabling direct syntheses of per(2-O-sulfonyl)-β-cyclodextrins;Tetrahedron Letters;2006-12
4. Synthesis of a Cycloallin Derivative from β-Cyclodextrin: Heptakis(2,3-dideoxy-2,3-epithio)-β-cycloallin;Angewandte Chemie International Edition;2005-07-04
5. Synthesis of a Cycloallin Derivative from β-Cyclodextrin: Heptakis(2,3-dideoxy-2,3-epithio)-β-cycloallin;Angewandte Chemie;2005-07-04
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