1-O-METHYL-2,3-O-ISOPROPYLIDENE-5-[4-(TETRAHYDRO-2-H-PYRAN)-METHYL)--1-H-1,2,3-TRIAZOL-1-YL]-BETA-D-RIBOFURANOSE
Compound with spectra: 1 NMR
![1-O-METHYL-2,3-O-ISOPROPYLIDENE-5-[4-(TETRAHYDRO-2-H-PYRAN)-METHYL)--1-H-1,2,3-TRIAZOL-1-YL]-BETA-D-RIBOFURANOSE](/api/compound/IQLQ7OUqZHb.png?ph=true&h=300&w=458 "1-O-METHYL-2,3-O-ISOPROPYLIDENE-5-[4-(TETRAHYDRO-2-H-PYRAN)-METHYL)--1-H-1,2,3-TRIAZOL-1-YL]-BETA-D-RIBOFURANOSE")
| SpectraBase Compound ID | IQLQ7OUqZHb |
|---|---|
| InChI | InChI=1S/C17H27N3O6/c1-17(2)25-14-12(24-16(21-3)15(14)26-17)9-20-8-11(18-19-20)10-23-13-6-4-5-7-22-13/h8,12-16H,4-7,9-10H2,1-3H3/t12-,13?,14-,15-,16-/m0/s1 |
| InChIKey | KBTPWTVSTNXJID-AOWBMEDYSA-N |
| Mol Weight | 369.42 g/mol |
| Molecular Formula | C17H27N3O6 |
| Exact Mass | 369.189986 g/mol |
| Enantiomer InChIKey | KBTPWTVSTNXJID-SLWHIKPQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-O-METHYL-2,3-O-ISOPROPYLIDENE-5-(4-PHENOXYMETHYL-1-H-1,2,3-TRIAZOL-1-YL)-BETA-D-RIBOFURANOSE
METHYL-5-DEOXY-5-C-(4-ETHOXYCARBONYL-1,2,3-TRIAZOL-1-YL)-2,3-O-ISOPROPYLIDENE-BETA-D-RIBOFUTANOSIDE
1-O-METHYL-2,3-O-ISOPROPYLIDENE-5-[4-(1-HYDROXY-1-METHYL-ETHYL)-1-H-1,2,3-TRIAZOL-1-YL]-BETA-D-RIBOFURANOSE
METHYL-5-DEOXY-5-C-(5-HXDROXYMETHYL-1,2,3-TRIAZOL-1-YL)-2,3-O-ISOPROPYLIDENE-BETA-D-RIBOFUTANOSIDE
5-(5-AMINO-4-CARBAMOYL-1,2,3-TRIAZOL-1-YL)-5-DEOXY-1,2-O-ISOPROPYLIDENE-ALPHA-D-RIBOFURANOSE
5-DEOXY-5-C-(5-ETHOXYCARBONYL-1,2,3-TRIAZOL-1-YL)-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSE
4-{[2'-Methoxy-5',5'-dimethyl-1',4',6'-trioxabicyclo[3.3.0]octyl]methoxycarbonyl}-2-methoxy-5.5-dimethyl-1,4,6-trioxabicyclo[3.3.0]octane
5-(5-AMINO-4-CARBAMOYLIMIDAZOL-1-YL)-5-DEOXY-1,2-ISOPROPYLIDENE-ALPHA-D-RIBOFURANOSE
Benzoyl 5-O-(tert-Butyldimethylsilyl)-3,4-O-isopropylidene-.alpha.-D-ribofuranose
Benzoyl 5-O-(tert-Butyldimethylsilyl)-3,4-O-isopropylidene-.beta.-D-ribofuranose
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis, Biological Activity, and Molecular Modeling Studies of 1H-1,2,3-Triazole Derivatives of Carbohydrates as α-Glucosidases Inhibitors | Journal of Medicinal Chemistry | 2010 |