5-epi-Deoxyrhamnojirimycin is a potent inhibitor of an α-l-rhamnosidase: 5-epi-deoxymannojirimycin is not a potent inhibitor of an α-d-mannosidase
- 21 August 1998
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 9 (16) , 2947-2960
- https://doi.org/10.1016/s0957-4166(98)00317-6
Abstract
No abstract availableKeywords
This publication has 75 references indexed in Scilit:
- Sugar mimics from sugar lactonesPublished by Walter de Gruyter GmbH ,1998
- Mechanism-based inhibition of carbohydrate-mediated biological recognitionsChemical Communications, 1998
- Indolizidine and quinolizidine alkaloidsNatural Product Reports, 1997
- Aldonolactones as chiral synthonsPublished by Springer Nature ,1997
- Synthesis of 1,6‐Dideoxynojirimycin, 1,6‐Dideoxy‐D‐allo‐nojirimycin, and 1,6‐Dideoxy‐D‐gulo‐nojirimycin via Asymmetric Hetero‐Diels‐Alder ReactionsHelvetica Chimica Acta, 1996
- Inhibitors of Glycosphingolipid Biosynthesis.Trends in Glycoscience and Glycotechnology, 1995
- Indolizidine and quinolizidine alkaloidsNatural Product Reports, 1994
- Chemical modification of azasugars, inhibitors of N‐glycoprotein‐processing glycosidases and of HIV‐I infection: Review and structure‐activity relationshipsRecueil des Travaux Chimiques des Pays-Bas, 1993
- Palladium-mediated stereocontrolled reductive amination of azido sugars prepared from enzymic aldol condensation: a general approach to the synthesis of deoxy aza sugarsJournal of the American Chemical Society, 1991
- (+)-Muscarine from L-rhamnoseJournal of the Chemical Society, Chemical Communications, 1991