[2S,3R,4S,5S,(7E)]-2,4-DIACETOXY-N-BENZYL-5-(TERT.-BUTYLDIPHENYLSILYLOXY)-8-PHENYL-3-(TOSYLAMINO)-OCT-7-ENAMIDE
Compound with spectra: 1 NMR
![[2S,3R,4S,5S,(7E)]-2,4-DIACETOXY-N-BENZYL-5-(TERT.-BUTYLDIPHENYLSILYLOXY)-8-PHENYL-3-(TOSYLAMINO)-OCT-7-ENAMIDE](/api/compound/IRuT1rX4q5x.png?ph=true&h=300&w=458 "[2S,3R,4S,5S,(7E)]-2,4-DIACETOXY-N-BENZYL-5-(TERT.-BUTYLDIPHENYLSILYLOXY)-8-PHENYL-3-(TOSYLAMINO)-OCT-7-ENAMIDE")
| SpectraBase Compound ID | IRuT1rX4q5x |
|---|---|
| InChI | InChI=1S/C48H54N2O8SSi/c1-35-30-32-40(33-31-35)59(54,55)50-44(46(57-37(3)52)47(53)49-34-39-22-13-8-14-23-39)45(56-36(2)51)43(29-19-24-38-20-11-7-12-21-38)58-60(48(4,5)6,41-25-15-9-16-26-41)42-27-17-10-18-28-42/h7-28,30-33,43-46,50H,29,34H2,1-6H3,(H,49,53)/b24-19+/t43-,44+,45+,46-/m0/s1 |
| InChIKey | TUZAEOPGFDWIRP-MSBBKBNTSA-N |
| Mol Weight | 847.1 g/mol |
| Molecular Formula | C48H54N2O8SSi |
| Exact Mass | 846.337014 g/mol |
| Enantiomer InChIKey | TUZAEOPGFDWIRP-VDLYOLQJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
benzoic acid, 2-[[3-[1-(3,4-dimethylphenyl)-3,4,6-trimethyl-1H-pyrazolo[3,4-b]pyridin-5-yl]-1-oxopropyl]amino]-, methyl ester
3-{1'-[4-(Dimethylamino)benzoyl]-2'-[4-(dimethylamino)benzylidene]hydrazino}-2-phenylinden-1-one
7-DEOXY-8-EPI-VALEROSIDATE-TETRAACETATE
7-DESOXY-8-EPI-VALEROSIDATE TETRAACETATE
(3R,4R,5R)-3-Azido-5-benzyloxy-N-[(1S)-1-(tert-butoxycarbonyl)-3-methylbutyl]-4-(o-nitrobenzenesulfonamido)piperidin-2-one
1,5-ANHYDRO-4-O-[3,4-BIS-O-(TERT.-BUTYLDIPHENYLSILYL)-6-DEOXY-2-PHENYLSELENO-BETA-GLUCO-PYRANOSYL]-2,6-DIDEOXY-L-ERYTHRO-HEX-1-EN-3-ULOSE
beta-D-glucopyranoside, 5-[2-(3,4-dimethoxyphenyl)ethyl]-4-methyl-4H-1,2,4-triazol-3-yl 2-(acetylamino)-2-deoxy-1-thio-, 3,4,6-triacetate
KANSHONE E
methyl (4E)-6-bromo-2-oxo-4-(1-oxo-3,4-dihydro-2(1H)-naphthalenylidene)-3,4-dihydro-2H-chromene-3-carboxylate
RAC-(1R,4S,4AR,9BS)-7,9-DIMETHOXY-1-(1-METHYLETHYL)-4-TOSYLOXYMETHYL-1,2,3,4,4A,9B-HEXAHYDRODIBENZOFURAN-4-OL
| Title | Journal or Book | Year |
|---|---|---|
| Enantiospecific Synthesis of a Protected Equivalent of APTO, the β-Amino Acid Fragment of Microsclerodermins C and D, by Aziridino-γ-lactone Methodology | European Journal of Organic Chemistry | 2009 |