Results 181 to 190 of about 31,939 (198)
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1959
A mixture of 87.2 g (0.5 mole) of methyl 5-(chloromethyl)-2-furoate (see p. 29), b.p. 114–116° /3 mm, and 300 ml of 90% acetic acid was prepared in a one-liter three-necked round-bottomed flask fitted with mercury-sealed stirrer and reflux condenser. The mixture was stirred while 98 g (1.5 g-atoms) of zinc dust was added in small portions over a period
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A mixture of 87.2 g (0.5 mole) of methyl 5-(chloromethyl)-2-furoate (see p. 29), b.p. 114–116° /3 mm, and 300 ml of 90% acetic acid was prepared in a one-liter three-necked round-bottomed flask fitted with mercury-sealed stirrer and reflux condenser. The mixture was stirred while 98 g (1.5 g-atoms) of zinc dust was added in small portions over a period
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Synthesis of methyl ethers of methyl (methyl ?-D-galactopyranosid)uronate
Chemistry of Natural Compounds, 1987E. V. Evtushenko, Yu. S. Ovodov
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The Partial Methylation of Methyl β-D-Xylopyranoside with Methyl Sulfate
Journal of the American Chemical Society, 1949O, WINTERSTEINER, A, KLINGSBERG
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