Enzymatic Preparation of Specifically Modified Linear Maltooligosaccharides through Porcine Pancreatic Amylase-Catalyzed Hydrolyses of Substituted γ-Cyclodextrins
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/5/19_5_743/_pdf
Reference21 articles.
1. 6A6B, 6A6C, and 6A6D-ditosylates of β-cyclodextrin
2. 6A6B-, 6A6C-, and 6A6D-disulfonates of .alpha.-cyclodextrin
3. Regiospecific A,B capping onto .beta.-cyclodextrin. Characteristic remote substituent effect on carbon-13 NMR chemical shift and specific Taka-amylase hydrolysis
4. Enzyme-based discrimination between clockwise and counterclockwise isomers of unsymmetrically disubstituted β-cyclodextrins. 6A,6B- and 6A,6G-derivatives
5. Regiospecific sulfonation of secondary hydroxyl groups of .alpha.-cyclodextrin. Its application to preparation of 2A2B, 2A2C-, and 2A2D-disulfonates
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Chemoenzymatic synthesis of 6ω-modified maltooligosaccharides from cyclodextrin derivatives;Carbohydrate Research;2005-08
2. Chemoenzymatic synthesis of modified maltooligosaccharides from cyclodextrin derivatives;Biochimie;1992-01
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