(3E,5E)-7,8,9-TRI-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-PYRROLIDINOMETHYL-D-ERYTHRO-NON-3,5-DIENE-2-ULOSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 93yRc4bsuIb |
|---|---|
| InChI | InChI=1S/C35H41NO4/c1-29(37)33(24-36-22-11-12-23-36)20-13-21-34(39-26-31-16-7-3-8-17-31)35(40-27-32-18-9-4-10-19-32)28-38-25-30-14-5-2-6-15-30/h2-10,13-21,34-35H,11-12,22-28H2,1H3/b21-13+,33-20-/t34-,35+/m1/s1 |
| InChIKey | PNGKRJSOGXYZHE-ZJBVJQFLSA-N |
| Mol Weight | 539.7 g/mol |
| Molecular Formula | C35H41NO4 |
| Exact Mass | 539.303559 g/mol |
| Enantiomer InChIKey | PNGKRJSOGXYZHE-XOZUDDFWSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3E,5E)-8-O-ACETYL-7,9-DI-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-DIETHYLAMINOMETHYL-D-THREO-NON-3,5-DIENE-2-ULOSE
(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
.alpha.-D-erythro-Hex-2-enopyranoside, phenyl 2,3-dideoxy-4,6-bis-O-(phenylmethyl)-
UYAWSMMZPIHXDH-XPWALMASSA-N
(4R,5S,6S)-1-TERT.-BUTYLDIMETHYLSILYLOXY-4,5,7-TRIBENZYLOXY-2E-HEPTEN-6-OL
(2R,3R,4R)-1,3,4-Tribenzyloxy-2-(p-methoxybenzyloxy)octadecane
3,4-DI-O-BENZYL-6-O-FORMYL-D-GLUCAL
(2S,3R,5Z,8S,9R)-2-ethenyl-8-phenylmethoxy-9-(phenylmethoxymethyl)-2,3,4,7,8,9-hexahydrooxonin-3-ol
Z-2,5-Anhydro-3-deoxy-4,6-di-O-benzyl-1-phenyl-D-ribo-hex-1-enitol
Methyl (2Z,4S,5S)-4-(4-Methoxybenzyloxy)-5,6-(pentylidenedioxy)hex-2-enoate
| 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 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.