305367-60-6Relevant academic research and scientific papers
Practical and convenient modifications of the A,C-secondary hydroxyl face of cyclodextrins
Teranishi, Katsunori
, p. 2519 - 2538 (2003)
A practical and convenient method for the preparation of α-, β-, and γ-cyclodextrin derivatives, in which the secondary hydroxyl faces of A- and C-glucose units are regioselectively modified, has been developed. Reactions of α-, β-, and γ-cyclodextrins wi
Regiospecific 2(A),2(C)-disulfonation of β-cyclodextrin
Teranishi
, p. 7085 - 7088 (2007/10/03)
The regiospecific 2(A),2(C)-disulfonation of β-cyclodextrin has been achieved by the reaction of β-cyclodextrin with 1,4-dibenzoylbenzene-3',3-disulfonyl imidazole and molecular sieves in DMF. (C) 2000 Elsevier Science Ltd.
