Tetrahedron Letters p. 8709 - 8712 (1997)
Update date:2022-07-29
Topics:
Matsushita, Yoh-Ichi
Sugamoto, Kazuhiro
Kita, Yoshio
Matsui, Takanao
1,2-Anhydro-3,4,6-tri-O-pivaloyl-α-D-glucopyranose (1a) was allowed to react with alcohols in the presence of solid acids such as silica gel and zeolite HY, to afford β-O-glucosides stereoselectively. Several natural glucosides were synthesized by the application of the present resection.
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