(3E,5E)-8-O-ACETYL-7,9-DI-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-PYRROLIDINOMETHYL-D-THREO-NON-3,5-DIENE-2-ULOSE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | IIdhPqfx2MP |
|---|---|
| InChI | InChI=1S/C30H37NO5/c1-24(32)28(20-31-18-9-10-19-31)16-11-17-29(35-22-27-14-7-4-8-15-27)30(36-25(2)33)23-34-21-26-12-5-3-6-13-26/h3-8,11-17,29-30H,9-10,18-23H2,1-2H3/b17-11+,28-16-/t29-,30-/m0/s1 |
| InChIKey | JEBVELFAMWAPJO-XNPGWVAMSA-N |
| Mol Weight | 491.6 g/mol |
| Molecular Formula | C30H37NO5 |
| Exact Mass | 491.267173 g/mol |
| Enantiomer InChIKey | JEBVELFAMWAPJO-UQECRBJTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3E,5E)-7,8,9-TRI-O-BENZYL-1,3,4,5,6-PENTADEOXY-3-PYRROLIDINOMETHYL-D-ERYTHRO-NON-3,5-DIENE-2-ULOSE
UYAWSMMZPIHXDH-XPWALMASSA-N
.alpha.-D-erythro-Hex-2-enopyranoside, phenyl 2,3-dideoxy-4,6-bis-O-(phenylmethyl)-
MXYLLYBWXIUMIT-HXMJJLHYSA-N
3,4,6-TRI-O-BENZYL-D-ALLAL;3,4,6-TRI-O-BENZYL-D-RIBO-HEX-1-ENITOL
MXYLLYBWXIUMIT-LLOGBAKRSA-N
3,4,6-TRI-O-BENZYL-D-GULAL;3,4,6-TRI-O-BENZYL-D-XYLO-HEX-1-ENITOL
(4R,5S,6S)-1-TERT.-BUTYLDIMETHYLSILYLOXY-4,5,7-TRIBENZYLOXY-2E-HEPTEN-6-OL
(4R,5S,6R)-1-TERT.-BUTYLDIMETHYLSILYLOXY-4,5,7-TRIBENZYLOXY-2E-HEPTEN-6-OL
METHYL-(4R,5S,6R)-6-HYDROXY-4,5,7-TRIBENZYLOXY-2Z-HEPTENOATE
| 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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