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The synthesis of tetrazoles derived from D-mannopyranose and D-rhamnopyranose from L-gulonolactone is described. These and other materials are assessed as inhibitors of human liver glycosidases and delineate some structural features required for α- and β-mannosidase and α-fucosidase inhibition. © 1995.

Original publication

DOI

10.1016/0040-4039(95)01519-1

Type

Journal article

Journal

Tetrahedron Letters

Publication Date

09/10/1995

Volume

36

Pages

7511 - 7514