Synthesis and enzyme-inhibitory activity of methyl acarviosin analogues having the α- manno configuration
- 1 March 1992
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 226 (1) , 79-89
- https://doi.org/10.1016/0008-6215(92)84056-x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Synthesis of a carba-sugar analog of trehalosamine, [(1S)-(1,2,43,5)-2-amino-3,4-dihydroxy-5-hydroxymethyl-1-cyclohexyl] α-d-glucopyranoside, and a revised synthesis of its β anomerCarbohydrate Research, 1990
- Synthesis of dl-2-amino-2-deoxyvalidamine and its three diastereoisomersCarbohydrate Research, 1990
- Synthesis of potent α-glucosidase inhibitors: methyl acarviosin analogue composed of 1,6-anhydro-β-D-glucopyranose residueJournal of the Chemical Society, Chemical Communications, 1990
- A practical, efficient large-scale synthesis of 1,6-anhydrohexopyranosesThe Journal of Organic Chemistry, 1989
- Total synthesis of (+)-pipoxide and (+)-.beta.-senepoxide and their diene precursorsThe Journal of Organic Chemistry, 1985
- Untersuchungen zur struktur des α-d-glucosidaseinhibitors acarboseCarbohydrate Research, 1984
- Synthesis and proof of structure of perosamine (4-amino-4,6-dideoxy-D-mannose) derivativesJournal of the American Chemical Society, 1970
- Selective acylation of pyranosides—II.Tetrahedron, 1967