A complete set of 6A-azido-6A-deoxy-6X-0-sulfonyl-β0-cyclodextrins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Cyclodextrin catalysis as a model for enzyme action
2. Artificial Enzymes
3. Design and synthesis of artificial enzymes
4. Regiospecific A,C- and A,D-disulfonate capping of .beta.-cyclodextrin
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1. A one-pot synthetic method for the hetero-bifunctionalization of α-cyclodextrin at the secondary hydroxyl side with high clockwise–counterclockwise selectivity;Organic & Biomolecular Chemistry;2017
2. γ-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives;Tetrahedron;2009-11
3. Hetero-bifunctional γ-cyclodextrins having dansylcysteine and tosyl groups at two adjacent sugar units: synthesis and determination of regio-chemistry;Tetrahedron Letters;2007-04
4. Selective modification of β-cyclodextrin: an unexpected tandem reaction enables the cross-linking of C2A and C2B via a sulfur atom;Chemical Communications;2007
5. 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
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