(3E,5E)-8-O-ACETYL-7-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-PIPERIDINOMETHYL-D-GLYCERO-OCT-3,5-DIENE-2-ULOSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 99HAU6mDG3V |
|---|---|
| InChI | InChI=1S/C23H31NO4/c1-19(25)22(16-24-14-7-4-8-15-24)12-9-13-23(18-27-20(2)26)28-17-21-10-5-3-6-11-21/h3,5-6,9-13,23H,4,7-8,14-18H2,1-2H3/b13-9+,22-12-/t23-/m1/s1 |
| InChIKey | SDAHDVKHSUKWQP-DWKWYLMZSA-N |
| Mol Weight | 385.5 g/mol |
| Molecular Formula | C23H31NO4 |
| Exact Mass | 385.225308 g/mol |
| Enantiomer InChIKey | SDAHDVKHSUKWQP-QGBHMSIFSA-N |
| Racemate InChIKey | SDAHDVKHSUKWQP-YAMRJJFBSA-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-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-PYRROLIDINOMETHYL-D-GLYCERO-OCT-3,5-DIENE-2-ULOSE
3-DEOXY-3-FLUORO-4-O-BENZYL-5-O-BENZOYL-D-XYLULOSE
(4E,6E,3S)-3-Benzyloxynona-4,6-dienyl toluene-p-sulfonate
3-DEOXY-3-FLUORO-4-O-BENZYL-5-O-BENZOYL-D-XYLITOL
(4R,5R)-4,5-bis(phenylmethoxy)-6-heptenoic acid tert-butyl ester
(2S,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
(2R,3R,E)-tert-butyl 3-(benzyloxy)-2-hydroxy-6-methylhept-4-enoate
(SYN)-(2S,3R,4R)-2-AMINO-3,4-DIBENZYLOXYHEX-5-ENENITRILE
(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 |
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.