Synthesis of 4-Carbamoyl-2-oxazolidinones C-4-Linked with a Saccharide Moiety via Bucherer-Bergs Reaction of Hexofuranos-5-uloses
Artikel i vetenskaplig tidskrift, 2002

Application of the Bucherer-Bergs reaction to 6-O-unprotected hexofuranos-5-uloses led to the formation of 4-carbamoyl-2-oxazolidinones C-4-linked with a carbohydrate moiety instead of expected carbohydrate-C-5-linked hydantoin (imidazolidin-2,4-dione) derivatives. Starting from hexofuranos-5-uloses having all hydroxyl groups suitably protected, only corresponding saccharide-linked hydandoins were obtained.

5-membered heterocycles

carbohydrates

5-hexofuranos-5-uloses

conjugation

Bucherer-Bergs reaction

Författare

Julia Micova

Bohumil Steiner

Miroslav Koos

Vratislav Langer

Chalmers, Institutionen för oorganisk miljökemi

Dalma Gyepesova

Synlett

0936-5214 (ISSN) 1437-2096 (eISSN)

Vol. 2002 10 1715-1717

Ämneskategorier

Kemi

DOI

10.1055/s-2002-34246