(5S,6R,7R,7AS)-6,7-DIBENZYLOXY-3-OXOTETRAHYDROPYRROLO-[1,2-C]-OXAZOLE-5-CARBONITRILE
Compound with spectra: 1 NMR
![(5S,6R,7R,7AS)-6,7-DIBENZYLOXY-3-OXOTETRAHYDROPYRROLO-[1,2-C]-OXAZOLE-5-CARBONITRILE](/api/compound/3HIhu5x3rgt.png?ph=true&h=300&w=458 "(5S,6R,7R,7AS)-6,7-DIBENZYLOXY-3-OXOTETRAHYDROPYRROLO-[1,2-C]-OXAZOLE-5-CARBONITRILE")
| SpectraBase Compound ID | 3HIhu5x3rgt |
|---|---|
| InChI | InChI=1S/C21H20N2O4/c22-11-17-19(25-12-15-7-3-1-4-8-15)20(18-14-27-21(24)23(17)18)26-13-16-9-5-2-6-10-16/h1-10,17-20H,12-14H2/t17-,18-,19+,20+/m0/s1 |
| InChIKey | OGRDPZXGHNLJCQ-VNTMZGSJSA-N |
| Mol Weight | 364.4 g/mol |
| Molecular Formula | C21H20N2O4 |
| Exact Mass | 364.142307 g/mol |
| Enantiomer InChIKey | OGRDPZXGHNLJCQ-ZRNYENFQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2R,3R,4S,5S)-N-BENZYL-3,4-BIS-(BENZYLOXY)-2-[(BENZYLOXY)-METHYL]-5-PROPYL-PYRROLIDINE-1-CARBOXAMIDE
(1R,2R,3R,5S,6R,7AR)-1,2-DIBENZYLOXY-3-(BENZYLOXYMETHYL)-6-HYDROXY-5-METHYLINDOLIZIDINE
4-(1,2-Bis-benzyloxy-3-oxo-propyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
6-O-ACETYL-2,4-DI-O-BENZYL-N-BENZYLOXYCARBONYL-1,5-DIDEOXY-1,5-IMINO-D-MANNITOL
(1R,2R,3R,5S,7S,8AR)-1,2-DIBENZYLOXY-3-(BENZYLOXYMETHYL)-7-HYDROXY-5-METHYLINDOLIZIDINE
(1R,2R,3R,5R,7S,8AR)-1,2-DIBENZYLOXY-3-(BENZYLOXYMETHYL)-7-HYDROXY-5-METHYLINDOLIZIDINE
(1L)-1, 2, 4/3, 5)-1,2-Anhydro-3, 4,5-tri-O-benzyl-2-carboxyamino-1-hydroxymethyl-3, 4, 5-cyclopentantriol(intramolekularer 2,1-Ester)
(1R,6S,7S,8R,8aS)-1-hydroxy-6,7,8-tri(benzyloxy)indolizidine
2-Deoxy-2-hexanoylamino-3,4,6-tri-O-benzyl-d-glucopyranose
Allyl-2-deoxy-2-hexanoylamino-3,4,6-tri-O-benzyl-b-d-allopyranoside
| Title | Journal or Book | Year |
|---|---|---|
| Stereoselective Strecker and Carbamate Annulation Methodology for the Synthesis of 1-Amino-1,2,5-trideoxy-2,5-imino-L-iditol | European Journal of Organic Chemistry | 2011 |