The acetonation of methyl 5-C-methoxy-beta-beta-d-galactopyranoside (1a), masked bis-glycoside form of L-arabino-hexos-5-ulose, with a large excess of 2,2-dimethoxypropane and catalytic amounts of p-toluenesulfonic acid gives a mixture of five acetonides. The most abundant isolated product was the mixed acetal methyl 6-O-(1-methoxy-1-methylethyl)-3,4-O-isopropylidene-5-C-methoxy-beta-d- galactopyranoside (44% yield).

The acetonation of methyl 5-C-methoxy-beta-D-galactopyranoside with 2,2-dimethoxypropane

CATELANI, GIORGIO;D'ANDREA, FELICIA;
1998-01-01

Abstract

The acetonation of methyl 5-C-methoxy-beta-beta-d-galactopyranoside (1a), masked bis-glycoside form of L-arabino-hexos-5-ulose, with a large excess of 2,2-dimethoxypropane and catalytic amounts of p-toluenesulfonic acid gives a mixture of five acetonides. The most abundant isolated product was the mixed acetal methyl 6-O-(1-methoxy-1-methylethyl)-3,4-O-isopropylidene-5-C-methoxy-beta-d- galactopyranoside (44% yield).
1998
Bergonzi, Mc; Catelani, Giorgio; D'Andrea, Felicia; DE RENSIS, F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/175713
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