Add time:08/25/2019         Source:sciencedirect.com

Efficient preparations both of 2,3:5,6:3′,4′-tri-O-isopropylidenelactose dimethyl acetal (5, 95% yield) and its 6′-O-(1-methoxy-1-methylethyl) derivative (65% yield), useful intermediates for the conversion of lactose into biologically relevant oligosaccharides, by ‘one-pot’ acetonation procedures with 2,2-dimethoxypropane are reported. The acetonation of 5 with 2-methoxypropene in the presence of pyridinium tosylate and 4 Å molecular sieves unexpectedly revealed the formation, in a first kinetic reaction phase, of similar amounts of the 2′-O- and 6′-O-(1-methoxy-1-methylethyl) acetals. The structures of all new products were fully characterized by NMR analyses, which also allowed some deductions on the conformation of the galactopyranosyl rings.

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