Title of article
Hydroxyl group orientation affects hydrolysis rates of methyl α-septanosides
Author/Authors
Markad، نويسنده , , Shankar D. and Miller، نويسنده , , Shawn M. and Morton، نويسنده , , Martha and Peczuh، نويسنده , , Mark W.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
4
From page
1209
To page
1212
Abstract
Hydrolysis rates for three related methyl α-septanosides were obtained. The septanosides were synthesized via mCPBA epoxidation and methanolysis of d-mannose, d-galactose, and d-glucose-based oxepines. The rate of hydrolysis correlates with the orientation of hydroxyl groups on the septanose ring in a manner analogous to pyranosides.
Journal title
Tetrahedron Letters
Serial Year
2010
Journal title
Tetrahedron Letters
Record number
1871268
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