(5E)-8-O-ACETYL-7,9-DI-O-BENZYL-1,3,5,6-TETRADEOXY-3-METHYLENE-D-LYXO/XYLO-NON-5-EN-2-ULOSE;MIXTURE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 90xjBPV6Ai1 |
|---|---|
| InChI | InChI=1S/C26H30O6/c1-19(20(2)27)24(29)14-15-25(31-17-23-12-8-5-9-13-23)26(32-21(3)28)18-30-16-22-10-6-4-7-11-22/h4-15,24-26,29H,1,16-18H2,2-3H3/b15-14+/t24?,25-,26-/m0/s1 |
| InChIKey | WBSUEJVNCRVUKA-OAZSBHDASA-N |
| Mol Weight | 438.52 g/mol |
| Molecular Formula | C26H30O6 |
| Exact Mass | 438.204239 g/mol |
| Enantiomer InChIKey | WBSUEJVNCRVUKA-BNBJXDJNSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
PROPAN-2-YL-4,6-DI-O-BENZYL-2,3-DIDEOXY-1-THIO-ALPHA-D-ERYTHRO-HEX-2-ENOPYRANOSIDE
(3E,5E)-7,8,9-TRI-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-DIETHYLAMINOMETHYL-D-ERYTHRO-NON-3,5-DIENE-2-ULOSE
OCTYL-4,6-DI-O-BENZYL-2,3-DIDEOXY-ALPHA-D-ERYTHRO-HEX-2-ENOPYRANOSIDE
(3R,4R,5R,6S)-3,4,5,6-Tetra(benzyloxy)cyclohexene
[(1R,2R,5R,6R)-2,5,6-tribenzoxycyclohex-3-en-1-yl]oxymethylbenzene
(3S*,4R*,5S*,6R*)-3,4,5,6-Tetra(benzyloxy)cyclohexene
1,3,4-tris(Benzyloxy)-5-docosen-2-ol
Z-2,5-Anhydro-3-deoxy-4,6-di-O-benzyl-1-phenyl-D-ribo-hex-1-enitol
()-Z(+/-)-(9S,10S)-9-chloroacetyl-10-(4-methoxybenzyloxy)-3,4,5,8,9,10-hexahydrooxecin-2-one
Benzyl 4,6-di-O-acetyl-2,3-dideoxy-a-D-erythro-hex-2-enopyranoside
| 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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