p-Tolyl 2,3-anhydro-5,6-O-isopropylidene-1-thio-β-D-gulofuranoside

被引：3

作者：

Bai, Y

Lowary, TL

Ferguson, MJ ^{[1
]}

机构：

[1] Univ Alberta, Dept Chem, Alberta Ingenuity Ctr Carbohydrate Sci, Edmonton, AB T6G 2G2, Canada

[2] Univ Alberta, Dept Chem, Xray Crystallog Lab, Edmonton, AB T6G 2G2, Canada

来源：

ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | 2004年 / 60卷

关键词：

D O I：

10.1107/S1600536804027266

中图分类号：

O7 [晶体学];

学科分类号：

0702 ; 070205 ; 0703 ; 080501 ;

摘要：

In the title compound, C16H20O4S, the epoxide ring is trans to the p-tolyl group and cis to the dioxolane moiety. The furanose ring adopts a conformation in which the furanose and epoxide O atoms are on the same face of the molecule (E-O) and the p-tolyl group adopts the conformation favored by the exoanomeric effect, gauche to the ring O atom and anti to the ring C atom.

引用

页码：O2201 / O2203

页数：3

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