(3E,5E)-8-O-ACETYL-7-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-PYRROLIDINOMETHYL-D-GLYCERO-OCT-3,5-DIENE-2-ULOSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | IzE01kpMWsS |
|---|---|
| InChI | InChI=1S/C22H29NO4/c1-18(24)21(15-23-13-6-7-14-23)11-8-12-22(17-26-19(2)25)27-16-20-9-4-3-5-10-20/h3-5,8-12,22H,6-7,13-17H2,1-2H3/b12-8+,21-11-/t22-/m0/s1 |
| InChIKey | LOPWOBFGXCEXJH-WXRAMUSKSA-N |
| Mol Weight | 371.48 g/mol |
| Molecular Formula | C22H29NO4 |
| Exact Mass | 371.209658 g/mol |
| Enantiomer InChIKey | LOPWOBFGXCEXJH-AUNCFCHGSA-N |
| Racemate InChIKey | LOPWOBFGXCEXJH-CFIKWKNBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-DEOXY-3-FLUORO-4-O-BENZYL-5-O-BENZOYL-D-XYLITOL
(4E,6E,3S)-3-Benzyloxynona-4,6-dienyl toluene-p-sulfonate
(4R,5R)-4,5-bis(phenylmethoxy)-6-heptenoic acid tert-butyl ester
(+-)-N-[(4-Benzyloxycyclopent-2-enyl)methyl]-benzamide
2-(1,2-DISTEAROYL-3-RAC-GLYCERO)-5-BENZYLOXY-1,3,2-DIOXAPHOSPHORINANE
(2R,3R,E)-tert-butyl 3-(benzyloxy)-2-hydroxy-6-methylhept-4-enoate
(2R,3S,Z)-tert-butyl 3-(benzyloxy)-2-hydroxy-6-methylhept-4-enoate
(2S,3R,E)-tert-butyl 3-(benzyloxy)-2-hydroxy-6-methylhept-4-enoate
(1S,2S,5R)-2-Benzyloxy-3,5-dimethylcyclohex-3-enol
(ANTI)-(2R,3R,4R)-2-AMINO-3,4-DIBENZYLOXYHEX-5-ENENITRILE
| Title | Journal or Book | Year |
|---|---|---|
| Baylis–Hillman Reaction: Convenient Ascending Syntheses and Biological Evaluation of Acyclic Deoxy Monosaccharides as Potential Antimycobacterial Agents | Bioorganic & Medicinal Chemistry | 2002 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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