139622-64-3Relevant academic research and scientific papers
Qualitative evaluation of regioselectivity in the formation of di- And tri-6-O-tritylates of α-cyclodextrin
Yoshikiyo, Keisuke,Matsui, Yoshihisa,Yamamoto, Tatsuyuki
, p. 1530 - 1540 (2016/04/09)
The quantitative analysis of reaction products showed that the reaction of 6A,6D-di-O-trityl-α-cyclodextrin (CD), AD-isomer, with trityl chloride in pyridine at 55 °C gave 6A,6B,6E-tri-O-trityl-α-CD, the amount of which was only 25% of that of simultaneou
Preparation of di-O-triphenylmethyl- (trityl-) cyclomaltohexaoses and -cyclomaltoheptaoses and characterization of three positional isomers of each by the 'hex-5-enose degradation'
Tanimoto,Tanaka,Yuno,Koizumi
, p. 1 - 10 (2007/10/02)
Regioisomeric 61,6(n)-di-O-trityl-cyclomaltohexaoses (cG6s) or -cyclomaltoheptaoses (cG7s) were prepared by the reaction of cyclomaltohexaose (1, cG6) or cylomaltoheptaose (5, cG7) with chlorotripheny
