UNTERSUCHUNGEN ZUR STRUCTUR DES α-D-GLUCOSIDASEINHIBITORS ACARBOSE

DOI: 10.1016/0008-6215(84)85333-1

Source and publish data:

Carbohydrate Research p. 235 - 268 (1984)

Update date:2022-08-05

Topics:

Authors:

Junge, Bodo

Heiker, Fred-R.

Kurz, Juergen

Mueller, Lutz

Schmidt,Delf D.

Wuensche, Christian

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Article abstract of DOI:10.1016/0008-6215(84)85333-1

Hydrolysis of the pseudotetrasaccharide acarbose (1), a potent inhibitor of intestinal α-D-glucosidases and effective oral antidiabetic agent, gave D-glucose and a tricyclic compound (1R,2S,3R,4aS,7R,8S,8aS,9aR)-1,2,3,4a,7,8,8a,9a-octahydro-1,2,7,8-tetrah

Full text of DOI:10.1016/0008-6215(84)85333-1

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