24904-92-5Relevant academic research and scientific papers
METHYLATION OF METHYL α-D-HEXOPYRANOSIDES WITH DIAZOMETHANE IN THE PRESENCE OF A SMALL AMOUNT OF WATER
Inoue, Yuko,Nagasawa, Kinzo
, p. 181 - 190 (2007/10/02)
The long-time reaction of methyl α-D-gluco-, α-D-manno-, and α-D-galactopyranosides with excess diazomethane-diethyl ether at 25 deg C the presence of water gave all partially methylated methyl α-D-hexopyranosides which differ in number and position of methyl substitution.The presence electrolytes, such as potassium or sodium phosphate, in the reaction medium enhanced the degree of methylation, resulting in preferential formation of tri-O-methyl derivatives of methyl α-D-hexopyranosides.
PARTIAL METHYLATION OF METHYL α-D-GLUCOPYRANOSIDE. I. LIQUID CHROMATOGRAPHY OF THE ACETATES OF THE TRI-O-METHYL ETHERS OF METHYL α-D-GLUCOPYRANOSIDE
Evtushenko, E. V.,Ovodov, Yu. S.
, p. 15 - 17 (2007/10/02)
A method is described for obtaining the acetates of the tri-O-methyl ethers of methyl α-D-glucopyranoside via the partial methylation of methyl α-D-glucopyranoside and the subsequent preparative liquid chromatography of the acetates of the tri-O-methyl ethers.
