scholarly journals Cleavage of the methylenedioxy group with sodium methoxide in dimethyl sulfoxide.

1978 ◽  
Vol 26 (10) ◽  
pp. 3113-3116 ◽  
Author(s):  
SHIGERU KOBAYASHI ◽  
MASARU KIHARA ◽  
YOSHINOBU YAMAHARA
1985 ◽  
Vol 16 (23) ◽  
Author(s):  
J. M. BARKER ◽  
P. R. HUDDLESTON ◽  
J. CLEPHANE ◽  
M. L. WOOD ◽  
D. HOLMES

1980 ◽  
Vol 33 (5) ◽  
pp. 1021 ◽  
Author(s):  
JL Frahn

Instructions are given for preparing the title compounds in reproducibly good yields from the appropriate anomer of methyl 4,6-O-benzylidene-2,3-di-O-tosyl-D-galactopyranoside. The α-anomer is converted into a mixture of the anhydro-α-taloside and anhydro-α- guloside by reaction with sodium methoxide in dimethyl sulfoxide as solvent at room temperature. The β-anomer forms the anhydro-β-taloside under similar conditions but with dioxan as solvent for the reactants.


1997 ◽  
Vol 62 (10) ◽  
pp. 1562-1576
Author(s):  
Petr Mitaš ◽  
Jaromír Kaválek ◽  
Oldřich Pytela

The dissociation constants of eleven amides have been measured in methanol and its mixtures with dimethyl sulfoxide (10 to 80% v/v) using sodium methoxide as the base. The experimental dissociation constants have been used to construct the H- acidity function as a function of methoxide concentration and composition of the DMSO-MeOH mixture as well as function of methoxide concentration in methanol. Moreover, with the help of construction of acidity function, the functions have been devised for constant sodium methoxide concentrations (0.025, 0.1, and 0.2 mol l-1) and changing composition of the DMSO-MeOH mixture.


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