Anomer-Selective Inhibition of Glycosidases Using Aminocyclopentanols
- 12 August 1999
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (5) , 775-777
- https://doi.org/10.1021/ol990754m
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- A Highly Efficient Pinacol Coupling Approach to Trehazolamine Starting from d-GlucoseThe Journal of Organic Chemistry, 1998
- Synthesis of Trehazolin from d-GlucoseThe Journal of Organic Chemistry, 1998
- Enantioselective Approaches to Aminocyclopentitols: A Total Synthesis of (+)-6-Epitrehazolin and a Formal Total Synthesis of (+)-TrehazolinThe Journal of Organic Chemistry, 1998
- 1-N-Iminosugars: Potent and Selective Inhibitors of β-GlycosidasesJournal of the American Chemical Society, 1998
- Synthesis of allosamidin analoguesCarbohydrate Research, 1996
- Comparison of a β-Glucosidase and a β-Mannosidase from the Hyperthermophilic Archaeon Pyrococcus furiosusJournal of Biological Chemistry, 1996
- Syntheses of the fungicide/insecticide allosamidin and a structural isomerJournal of the Chemical Society, Perkin Transactions 1, 1994
- Configurationally selective transition state analogue inhibitors of glycosidases. A study with nojiritetrazoles, a new class of glycosidase inhibitorsCarbohydrate Research, 1993
- Synthesis of AllosamidinHelvetica Chimica Acta, 1992
- Efficient enantioselective syntheses of carbocyclic nucleoside and prostaglandin synthonsTetrahedron Letters, 1990