103814-18-2Relevant academic research and scientific papers
A complete set of β-cyclodextrins 6(A),6(X)-diactivated by two different sulfonyl groups
Fujita,Yamamura,Imoto
, p. 6737 - 6740 (2007/10/02)
Each of 6(A)-0-(p-nitrobenzenesulfonyl)-6(X)-O-(β-naphthalenesu lfonyl)-β-cyclodextrins (X=B-G) was prepared by the reaction of 6-O-(β-naphthalenesulfonyl)-β-cyclodextrin with p-nitrobenzenesulfonyl chloride, isolated, and structurally determined through
ENZYME-BASED DISCRIMINATION BETWEEN CLOCKWISE AND COUNTERCLOCKWISE ISOMERS OF UNSYMMETRICALLY DISUBSTITUTED β-CYCLODEXTRINES. 6A,6B- AND 6A,6G-DERIVATIVES
Fujita, Kahee,Natsunaga, Atsuo,Ikeda, Yoshiko,Imoto, Taiji
, p. 6439 - 6442 (2007/10/02)
6A,6X-Dideoxy-6A-phenylthio-6X--β-cyclodextrins (X=G and B) (5 and 6) were prepared together with the other isomers (X=C, D, E, and F) (1-4), isolated by reversed-phase column chromatography, and structurally assigned by use of Taka amylolysis.
