Identification of the 2-hydroxymethyl-3,4-dihydroxypyrrolidine (or 1,4-dideoxy-1,4-iminopentitol) from and from as the (2R, 3R, 4S)-isomer by the synthesis of its enantiomer.
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (26), 3125-3126
- https://doi.org/10.1016/s0040-4039(00)98635-0
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- 3,4-dihydroxy-2-hydroxymethylpyrrolidine from Arachniodes standishiiPhytochemistry, 1985
- Carbohydrate triflates: Introduction of substituents by double inversion at C-4″ of kanamycin ACarbohydrate Research, 1984
- Inhibitors of trimming: new tools in glycoprotein researchTrends in Biochemical Sciences, 1984
- Glucosidase and trehalase inhibition by 1,5-dideoxy-1,5-imino-D-mannitol, a cyclic amino alditol from Lonchocarpus sericeusPhytochemistry, 1983
- Conversion of hydroxyl groups into bromo groups in carbohydrates with inversion of configurationCanadian Journal of Chemistry, 1981
- Glucosidase-Inhibitoren aus BazillenThe Science of Nature, 1979
- Isolation and structure of an unusual cyclic amino alditol from a legumeJournal of the Chemical Society, Chemical Communications, 1979
- Pyrrolodine sugars. Synthesis of 9-(4-acetamido-4-deoxy-.beta.-D-xylofuranosyl)adenine and other derivatives of 4-amino-4-deoxy-D-xyloseThe Journal of Organic Chemistry, 1967