31506-20-4Relevant academic research and scientific papers
Regioselective methylation of methyl glycopyranosides with diazomethane in the presence of transition-metal chlorides and of boric acid
Evtushenko, Evgeny V.
, p. 187 - 200 (2007/10/03)
Partial methylation of the methyl pyranosides of a number of pentoses, hexoses, 6-deoxyhexoses, methyl uronates and their methyl ethers with diazomethane in the presence of transition-metal chlorides and boric acid was studied. It was found for methyl glycosides of pentoses and 6-deoxyhexoses that tin(II), antimony(III), and titanium(IV) chlorides as well as boric acid promoted substitution mainly of OH-3, but with cerium(III) and zinc(II) salts mainly substitution of OH-2 was observed. Methylation of methyl β-l-rhamnopyranoside demonstrated higher reactivity of OH-2 in all cases. The methylation of methyl glycosides of hexoses in the presence of tin(II), antimony(III) and cerium(III) chlorides gave mainly 3-methyl ethers. The 3-methyl ethers, which are not involved in further complexation, accumulated up to 50-80% of the reaction mixture (95-100% of monomethyl ether fraction). Convenient preparative syntheses of methyl ethers for a number of sugars are suggested. Copyright (C) 1999 Elsevier Science Ltd.
SYNTHESIS OF METHYL ETHERS OF METHYL (METHYL α-D-GLUCOPYRANOSID) URONATE
Evtushenko, E. V.,Ovodov, Yu. S.
, p. 26 - 28 (2007/10/02)
Methyl (methyl α-D-glucopyranoisid)uronate (I) has been obtained by the catalytic oxidation of methyl α-D-glucopyranoside with oxygen in the presence of platinum on carbon with a yield of 31percent.The partial methylation of (I) followed by preparative liquid column chromatography on silica gel has provided a convenient method of obtaining all the methyl ethers of (I) in the individual state.
