153697-29-1Relevant academic research and scientific papers
Efficient and Regioselective Preparation of an Eight-membered Interglycosidic Benzylidene Derivative of β-Cyclodextrin
Sakairi, Nobuo,Kuzuhara, Hiroyoshi
, p. 2077 - 2080 (1993)
Heptakis(6-O-pivaloyl)-β-cyclodextrin, prepared in high yield by pivaloylation of β-cyclodextrin (β-CD), was treated with α,α-dimethoxytoluene in the presence of (+)-10-camphorsulfonic acid to give a 46percent yield of eight-membered interglycosidic benzy
Regioselective synthesis of methylated β-cyclodextrins leaving hydroxy groups
Matsuoka, Koji,Shiraishi, Yoko,Terunuma, Daiyo,Kuzuhara, Hiroyoshi
, p. 1531 - 1533 (2007/10/03)
A series of methylated β-cyclodextrins (CDs) regioselectively leaving one or two hydroxy groups were prepared, and fluorescence spectroscopic measurements showed that they have unique binding characteristics against 2-p-toluidinylnaphthalene-6-sulfonate as a guest molecule in aqueous solution.
