(3S,4R,5S)-3-ACETOXY-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-4-(TOSYLAMINO)-TETRAHYDROFURAN-2-ONE
Compound with spectra: 1 NMR
![(3S,4R,5S)-3-ACETOXY-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-4-(TOSYLAMINO)-TETRAHYDROFURAN-2-ONE](/api/compound/HRpaiXKiUk0.png?ph=true&h=300&w=458 "(3S,4R,5S)-3-ACETOXY-5-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-4-(TOSYLAMINO)-TETRAHYDROFURAN-2-ONE")
| SpectraBase Compound ID | HRpaiXKiUk0 |
|---|---|
| InChI | InChI=1S/C30H35NO7SSi/c1-21-16-18-23(19-17-21)39(34,35)31-27-26(38-29(33)28(27)37-22(2)32)20-36-40(30(3,4)5,24-12-8-6-9-13-24)25-14-10-7-11-15-25/h6-19,26-28,31H,20H2,1-5H3/t26-,27-,28+/m1/s1 |
| InChIKey | JLWKHYWGBFHWJP-FCEKVYKBSA-N |
| Mol Weight | 581.8 g/mol |
| Molecular Formula | C30H35NO7SSi |
| Exact Mass | 581.19035 g/mol |
| Enantiomer InChIKey | JLWKHYWGBFHWJP-HZFUHODCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,4S,5S)-6-(BENZYLOXYCARBONYL)-4-[(TERT.-BUTYLDIPHENYLSILYLOXY)-METHYL]-3-OXA-6-AZA-BICYCLO-[3.1.0]-HEXAN-2-ONE
5'-O-[(TERT.-BUTYL)-DIPHENYLSILYL]-1',2'-O-ISOPROPYLIDENE-BETA-D-ARABINOFURANOSIDE-3'H-PHOSPHONATE-TRIETHYLAMMONIUM-SALT
5'-O-[(TERT.-BUTYL)-DIPHENYLSILYL]-1',2'-O-ISOPROPYLIDENE-BETA-D-ARABINOFURANOSIDE-3'-PHOSPHATE-BIS-SODIUM-SALT
(2R,3R,4S,5S,6S)-6-tert-Butyldiphenylsilyloxymethyl-3,5-diacetoxy-2-methoxy-4-methyl-3,4,5,6-tetrahydro-2H-pyran
1-{2-DEOXY-5-O-[(1,1-DIMETHYLETHYL)-DIPHENYLSILYL]-BETA-D-ERYTHRO-PENTOFURANOSYL}-1H-PYRROLO-[2,3-B]-PYRIDINE
(2SR,4S,5S)-5-{[(tert-Butyldiphenylsilyl)oxy]methyl}-4-(but-3-ynyl)-1-tosylpyrrolidin-2-ol
3-O-BENZYL-5-O-TERT.-BUTYL-DIPHENYLSILYL-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSE
1-(3-AZIDO-5-O-TERT.-BUTYLDIPHENYLSILYL-2,3-DIDEOXY-BETA-D-ERYTHRO-PENTOFURANOSYL)-2-THIOURACIL
1-(3-AZIDO-5-O-TERT.-BUTYLDIPHENYLSILYL-2,3-DIDEOXY-ALPHA-D-ERYTHRO-PENTOFURANOSYL)-2-THIOURACIL
METHYL-3-O-BENZOYL-6-O-(TERT.-BUTYLDIPHENYLSILYL)-2,4-DIDEOXY-4-C-[(METHOXYCARBONYL)-METHYL]-ALPHA-D-RIBO-HEXOPYRANOSIDE
| 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 |