An expeditious synthesis of a (3S,4S,5R)-trihydroxyazepane
- 29 August 2003
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 44 (39), 7321-7323
- https://doi.org/10.1016/s0040-4039(03)01870-7
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Polyhydroxylated azepanes as new motifs for DNA minor groove binding agentsBioorganic & Medicinal Chemistry Letters, 2001
- Synthesis of azasugars as potent inhibitors of glycosidasesBioorganic & Medicinal Chemistry, 1997
- C2-Symmetrical tetrahydroxyazepanes as inhibitors of glycosidases and HIV/FIV proteasesBioorganic & Medicinal Chemistry, 1996
- Synthesis of azasugars. Part 2 isomerization of polyhydroxylated azepanesTetrahedron Letters, 1996
- Enzymatic/Chemical Synthesis and Biological Evaluation of Seven-Membered IminocyclitolsJournal of the American Chemical Society, 1996
- Unprecedented Selectivity in the Reaction of 1,2:5,6-Dianhydro-3,4-O- Isopropylidenehexitols with Benzylamine: A Practical Synthesis of 3,4,5,6-TetrahydroxyazepanesThe Journal of Organic Chemistry, 1995
- Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition (Part 2)Angewandte Chemie International Edition in English, 1995
- Polyhydroxylated piperidines and azepanes from D-mannitol synthesis of 1-deoxynojirimycin and analoguesTetrahedron Letters, 1994
- Amino-sugar glycosidase inhibitors: versatile tools for glycobiologistsGlycobiology, 1992
- On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functionsTetrahedron, 1986