104867-16-5Relevant articles and documents
Remarkably enhanced excimer formation of naphthylacetate in cation-charged gamma-cyclodextrin.
Ikeda, Hiroshi,Iidaka, Yoshiko,Ueno, Akihiko
, p. 1625 - 1627 (2003)
[reaction: see text] 6(A),6(D)-Bispyridinio-appended gamma-cyclodextrin effectively enhanced the excimer fluorescence of 2-naphthylacetate. This increase derived from the increase of formation of the 1:2 complex between the cation-charged gamma-cyclodextrin and 2-naphthylacetate by the electrostatic interaction between the host and the guest.
Synthesis of 6A,6X-Di-O-(p-tosyl)-γ-cyclodextrins and Their Structural Determination through Enzymatic Hydrolysis of 3A,6A;3X,6X-Dianhydro-γ-cyclodextrins
Fujita, Kahee,Yamamura, Hatsuo,Imoto, Taiji,Fujioka, Toshiro,Mihashi, Kunihide
, p. 1943 - 1947 (2007/10/02)
6A,6X-Di-O-(p-tosyl)-γ-cyclodextrins (X = B, C, D, and E) were prepared by the reaction of γ-cyclodextrin and p-tosyl chloride in pyridine and isolated by reversed-phase column chromatography.From the results of Taka amylolyses of 3A,6A;3X,6X-dianhydro-γ-cyclodextrins which were obtained from the corresponding ditosylates, the regiochemistry of the ditosylates was determined.