(3Z,5E)-8-O-ACETYL-7,9-DI-O-BENZYL-3-CHLOROMETHYL-1,3,4,5,6-PENTADEOXY-D-THREO-NON-3,5-DIENE-2-ULOSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 41GQxrdkkbf |
|---|---|
| InChI | InChI=1S/C26H29ClO5/c1-20(28)24(16-27)14-9-15-25(31-18-23-12-7-4-8-13-23)26(32-21(2)29)19-30-17-22-10-5-3-6-11-22/h3-15,25-26H,16-19H2,1-2H3/b15-9+,24-14+/t25-,26-/m0/s1 |
| InChIKey | ZSSWKLBEQYAMEW-VOHNSAGMSA-N |
| Mol Weight | 456.97 g/mol |
| Molecular Formula | C26H29ClO5 |
| Exact Mass | 456.170352 g/mol |
| Enantiomer InChIKey | ZSSWKLBEQYAMEW-VWCBFRSPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3Z,5E)-7,8,9-TRI-O-BENZYL-3-CHLOROMETHYL-1,3,4,5,6-PENTADEOXY-D-ERYTHRO-NON-3,5-DIENE-2-ULOSE
(4R,5S,6R)-4,5,7-TRIBENZYLOXY-2E-HEPTEN-1,6-DIOL
(2E,4S,5S)-1-Hydroxy-2-methyl-4,5-O-isopropylidene-6-benzyloxy-4,5-hex-2-enediol
1,2,3,5-Tetra-O-Benzyl-4-O-formyl-D-arabinitol
1,5-Anhydro-4,6-di-O-benzyl-2,3-dideoxy-2-C-formyl-D-erythro-hex-1-enitol
1,5-Anhydro-4,6-di-O-benzyl-2,3-dideoxy-2-C-formyl-D-threohex-1-enitol
1-[O-(Benzyloxy)-5-phenyl-4-pentene-1,2-diol - acetonide
3,4-DI-O-BENZYLGLUCAL
1,3,4,6-TETRA-O-BENZYL-2,5-ANHYDRO-D-GLUCITOL
(2E)-4,5,6-TRI-O-ACETYL-1,2,3-TRIDEOXY-1-(N-PROPARGYL-TERT.-BUTYLOXYCARBONYLAMINE)-D-ERYTHRO-HEX-2-ENOSE
| 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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