An improved and general synthesis of N-glycosylated oxindoles by SET-reduction of isatin-N-glycosides

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Authors: Martin Hein, Anna Frey, Dirk Michalik, Peter Ehlers, Peter Langer
Cited by: 0
References: 41

Abstract

Oxindole- N -glycosides were efficiently prepared by reduction of acetyl- and formyl protected isatin- N -glycosides with low-valent titanium and following cleavage of the protecting groups under basic conditions. The products could be isolated as pure anomers – no noticeable anomerization took place. • A variety of oxindole- N -glycosides were efficiently prepared from readily available starting materials. • The products were isolated as pure anomers. • Products could be deprotected and are not readily available by other methods.

Fields of Study & Subjects

Carbohydrate Chemistry and Synthesis Glycosylation and Glycoproteins Research Synthesis of Indole Derivatives

Publication details

Journal / source
Tetrahedron Letters
Volume
178
Pages
156004–156004
Publication date
12 February 2026
Language
EN