(2S)-2-[(1R)-1-[(1R)-2-OXO-1-(2-BROMOPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER
Compound with spectra: 1 NMR
![(2S)-2-[(1R)-1-[(1R)-2-OXO-1-(2-BROMOPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER](/api/compound/1BIlErCetws.png?ph=true&h=300&w=458 "(2S)-2-[(1R)-1-[(1R)-2-OXO-1-(2-BROMOPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER")
| SpectraBase Compound ID | 1BIlErCetws |
|---|---|
| InChI | InChI=1S/C24H33BrN2O4/c1-5-17(19-12-10-16-27(19)23(29)31-24(2,3)4)21(22(28)26-14-8-9-15-26)30-20-13-7-6-11-18(20)25/h5-7,11,13,17,19,21H,1,8-10,12,14-16H2,2-4H3/t17-,19+,21-/m1/s1 |
| InChIKey | CAXPGZNQGIODMU-SLYNCCJLSA-N |
| Mol Weight | 493.4 g/mol |
| Molecular Formula | C24H33BrN2O4 |
| Exact Mass | 492.162371 g/mol |
| Enantiomer InChIKey | CAXPGZNQGIODMU-DSKINZAPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
tert-Butyl (2S,3S,4aS,5R,8aR)-3-{[tert-Butyl(dimethyl)silyl]oxy}-5-(hydroxymethyl)-2-methyloctahydro-1(2H)-quinolinecarboxylate
Ethyl 5-carbomoyl-6-oxo-4-(phenyl)-2-trifluoromethyl-1,4,5,6-tetrahydropyridine-3-carboxylate
4-ALLYLOXYPHENYL-2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
2-phenylethyl 1,6-dimethyl-4-(5-methyl-2-thienyl)-2-oxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate
3-PENTAFLUOROPHENOXY-6-CHLORO-PERFLUORO-2,4-CYCLOHEXADIENONE
3-PHENYL-5-PENTAFLUOROPHENYL-6-CARBOETHOXY-2-CYCLOHEXENONE
(4R,5S)-5-Azido-4-(4-methoxyphenyl)-6-oxo-6-[(4S)-(2-oxo-4-phenyloxazolidin-3-yl)]hexanoic acid tert-Butyl ester
4-{(5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)[2-(trifluoromethyl)phenyl]methyl}-3-methyl-1-phenyl-1H-pyrazol-5-ol
3-Oxa-6-azabicyclo[3.2.2]nonane-6,7-dicarboxylic acid, 2-oxo-, 7-methyl 6-(phenylmethyl) ester, (1.alpha.,5.alpha.,7.alpha.)-
Methyl 5-(4-methoxy-2-methoxy carbonyl phenoxy)-4-methoxy carbonyl-3-hydroxy benzoic acid
| Title | Journal or Book | Year |
|---|---|---|
| 1,2-Asymmetric Induction in Diastereoselective Zwitterionic Aza-Claisen Rearrangements: Key Steps in Optically Active Alkaloid Synthesis | European Journal of Organic Chemistry | 2013 |