Interglucosyl Attack of Hydroxyl Group to Epoxy Ring of 2A,3A-Anhydro-(2AS)-α-cyclodextrin. Selective Preparation of 3A,2B-Anhydro-α-cyclodextrin
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/18/5/18_5_917/_pdf
Reference7 articles.
1. Synthesis of 6A,6X-di-O-(p-tosyl)-.gamma.-cyclodextrins and their structural determination through enzymic hydrolysis of 3A,6A;3X,6X-dianhydro-.gamma.-cyclodextrins
2. Regiospecific sulfonation of secondary hydroxyl groups of .alpha.-cyclodextrin. Its application to preparation of 2A2B, 2A2C-, and 2A2D-disulfonates
3. Synthesis of specifically modified maltooligosaccharides by enzymic degradation of cyclodextrin derivatives. Substrate-based investigation of the active site of Taka-amylase
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1. Selective synthesis and ester cleavage property of 3A,2B-anhydro-3B-deoxy-3B-thio-β-cyclodextrin;Tetrahedron Letters;2007-10
2. Construction of a Fused Polycyclic Wall within the Cyclodextrin Belt To Ensure a Distorted Cavity: An Unusualtrans-Diequatorial Ring-Opening Reaction of Cyclodextrin Epoxide Rings;European Journal of Organic Chemistry;2004-07
3. Functionalization of Cyclodextrins via Reactions of 2,3-Anhydrocyclodextrins;The Journal of Organic Chemistry;2003-10-29
4. Capped Cyclodextrins;Chemical Reviews;2003-10-17
5. Two stereoisomeric 3I,2II-anhydro-α-cyclodextrins: a molecular dynamics and crystallographic study;Carbohydrate Research;2001-12
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