T. Yamanoi, A. Fujioka, T. Inazu
May 1, 1994
Citations
0
Influential Citations
15
Citations
Journal
Bulletin of the Chemical Society of Japan
Abstract
The reactions of 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl dimethylphosphinothioate and phenolic compounds gave the corresponding aryl α-D-glucopyranosides predominantly in good yields, even when the trimethylsiloxy derivatives of benzene, which are known to afford 1-aryl-1-deoxy-D-glucopyranoses by the conventional methods, were used as acceptors. On the other hands, 1-ary-1-deoxy-β-D-glucopyranose was obtained in good yield when 1,3,5-trimethoxybenzene was used as an acceptor.