JWXHKWBUBUUEFP-SNSGHMKVSA-N
Compound with spectra: 3 NMR
| SpectraBase Compound ID | Lu9GZvDPHtA |
|---|---|
| InChI | InChI=1S/C35H36O6/c36-31-21-35(37,26-38-22-27-13-5-1-6-14-27)34(41-25-30-19-11-4-12-20-30)33(40-24-29-17-9-3-10-18-29)32(31)39-23-28-15-7-2-8-16-28/h1-20,32-34,37H,21-26H2/t32-,33+,34-,35-/m0/s1 |
| InChIKey | JWXHKWBUBUUEFP-SNSGHMKVSA-N |
| Mol Weight | 552.7 g/mol |
| Molecular Formula | C35H36O6 |
| Exact Mass | 552.251189 g/mol |
| Enantiomer InChIKey | JWXHKWBUBUUEFP-AOJHZZQJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
- 2,3,4,7-TETRA-O-BENZYL-[1-(13)C]-VALIOLONE
- (1S)-(1-(OH),2,4/1,3)-2,3,4-TRI-O-BENZYL-1-C-[(BENZYLOXY)-METHYL]-5-OXO-1,2,3,4-CYCLOHEXANETETROL
1,3,4,5,6-PENTA-O-BENZYL-2-C-TRICHLOROMETHYL-MYO-INOSITOL
(4S,5S,6S)-4-[(1E)-1,5-dimethyl-1,4-hexadienyl]-5,6-bis[(4-methoxybenzyl)oxy]-1-oxaspiro[2.5]octane
(2S,4aS,6R,7R,8S,8aS)-7,8-bis(benzyloxy)-6-(benzyloxymethyl)-2-(but-3-enyl)hexahydropyrano[3,2-b]pyran-3(2H)-one
1,6-ANHYDRO-TRI-O-BENZYL-5-HYDROXY-BETA-L-IDOPYRANOSIDE
3,4,5-TRI-O-BENZYL-7-DEOXY-7-FLUORO-D-GLYCERO-ALPHA-D-LYXO-HEPT-2-ULOPYRANOSIDE
1,3-Dioxolo[4,5-c]pyran, tetrahydro-, 7-(2-acetoxyethyl)-7-hydroxy-2,2-dimethyl-4-(3-methoxycarbonyl-2-methylallyl)-
(2R,3R,5R,6R)-2,6-DIBENZYLOXY-8-BROMO-5-(TERT.-BUTYLDIMETHYLSILOXY)-3-(PARA-METHOXYBENZYLOXY)-4,4-DIMETHYL-7-OXOOCTANAL
(2R,3S,4S,5R)-3,4,5-TRIS-(BENZYLOXY)-2-((BENZYLOXY)-METHYL)-6-ETHOXY-2,3,4,5-TETRAHYDROPYRIDINE
| Title | Journal or Book | Year |
|---|---|---|
| 1-Silyl-2,6-diketones: Versatile Intermediates for the Divergent Synthesis of Five- and Six-Membered Carbocycles under Radical and Anionic Conditions | Organic Letters | 2006 |
| Biosynthetic Studies on the α-Glucosidase Inhibitor Acarbose in Actinoplanes sp.: 2-epi-5-epi-Valiolone Is the Direct Precursor of the Valienamine Moiety | Journal of the American Chemical Society | 1999 |
| Synthesis of a branched-chain inosose derivative, a versatile synthon of N-substituted valiolamine derivatives from D-glucose | The Journal of Organic Chemistry | 1992 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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