2-(3',4',6'-TRI-O-BENZYL-2'-DEOXY-BETA-D-ARABINO-HEXOPYRANOSYL)-5,8-DIMETHOXYNAPHTHALEN-1-OL
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | IB0QSol5LmY |
|---|---|
| InChI | InChI=1S/C39H40O7/c1-41-32-20-21-33(42-2)37-30(32)18-19-31(38(37)40)34-22-35(44-24-28-14-8-4-9-15-28)39(45-25-29-16-10-5-11-17-29)36(46-34)26-43-23-27-12-6-3-7-13-27/h3-21,34-36,39-40H,22-26H2,1-2H3/t34-,35-,36-,39+/m1/s1 |
| InChIKey | BPBGAKROVZQJGM-DWRYXRPYSA-N |
| Mol Weight | 620.7 g/mol |
| Molecular Formula | C39H40O7 |
| Exact Mass | 620.277404 g/mol |
| Enantiomer InChIKey | BPBGAKROVZQJGM-USDDEDAYSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | K-2001-1630-19 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 1-Hydroxy-5,8-dimethoxy-2-(3',4',6'-tri-O-benzyl-2'-deoxy-.beta.,D-arabino-hexopyranosyl)naphthalene
2-(3',4',6'-TRI-O-ACETYL-2'-DEOXY-BETA-D-ARABINO-HEXOPYRANOSYL)-5,8-DIMETHOXYNAPHTHALEN-1-OL
8-Hydroxy-1,5-dimethoxy-2-(3',4',6'-tri-O-benzyl-2'-deoxy-.beta.,D-arabino-hexopyranosyl)naphthalene
2,2'-[(3R*,4S*,5S*)-3,4,5-TRIACETOXY-6,6,6-TRIFLUOROHEXYLIDENE]-BIS-(5,8-DIMETHOXYNAPHTHALEN-1-OL)
2,3,5-TRICHLORO-6-(1-HYDROXY-5,8-DIMETHOXYNAPHTHALEN-2-YL)-[1,4]-BENZOQUINONE
2-[(2S,3R,5R)-2-benzoxy-5-[tert-butyl(dimethyl)silyl]oxy-1-hydroxy-3-triethylsilyloxy-hexyl]-4,8-dimethoxy-1-naphthol
2-O-[2-(AZIDOMETHYL)-BENZOYL]-3,4,6-TRI-O-BENZYL-BETA-D-GLUCOPYRANOSYL-(1->6)-1,2:3,4-DIISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOSIDE
2-ACETYL-7-(1-HYDROXY-4,8-DIMETHOXY-7-NAPHTHYL)-4,8-DIMETHOXY-1-NAPHTHOL
;#40;ALLYL-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-[2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANO
10,11-Dibromo-9-acetoxy-10,11-dihydro-6'-methoxycinchonane
2,3-Dihydro-2,2,2-triphenylphenanthro[9,10-d]-1,3,2.lambda.(5)-oxazaphosphole
| Title | Journal or Book | Year |
|---|---|---|
| Synthetic Approaches to the Angucycline Antibiotics. A Route to C-Glycosidic Benz[a]anthraquinones | Australian Journal of Chemistry | 2000 |
This compound is available in the following databases:
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