"Dihydroacarbose" (2), an alpha-D-glucosidase inhibitor having a pseudo-tetrasaccharide structure, was synthesized by reductive coupling of 4(3)-amino-1(1),6(1)-anhydro-2(1),3(1),2(2),3(2),6(2),2(3),3(3)-hepta-O- benzyl-4(3),6(3)-dideoxy-beta-maltotriose and 2D-(2,4/3,5)-2,3,4-tris(benzyloxy)-5-(tri
✦ LIBER ✦
Synthesis of a 4′-amino-4′,6′-dideoxymaltose derivative as a synthon of an α-d-glucosidase inhibitor
✍ Scribed by Nobuo Sakairi; Hideo Murakami; Hiroyoshi Kuzuhara
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 465 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0008-6215
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