(4S,1'R)-(1'-Ethoxycarbonylmethyl-4'-phenylbutyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
Compound with spectra: 2 NMR
| SpectraBase Compound ID | 974xPsaiOrH |
|---|---|
| InChI | InChI=1S/2C24H37NO5/c2*1-7-28-21(26)16-19(15-11-14-18-12-9-8-10-13-18)20-17-29-24(5,6)25(20)22(27)30-23(2,3)4/h2*8-10,12-13,19-20H,7,11,14-17H2,1-6H3/t19-,20+;19-,20-/m01/s1 |
| InChIKey | AIZSGFXVKMRLHJ-GURKPNMWSA-N |
| Mol Weight | 839.1 g/mol |
| Molecular Formula | C48H74N2O10 |
| Exact Mass | 838.534347 g/mol |
| Enantiomer InChIKey | AIZSGFXVKMRLHJ-NEKPRPMVSA-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 |
- (4S,1'S)-(1'-Ethoxycarbonylmethyl-4'-phenylbutyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
2-[(4S,5S)-2,2-dimethyl-3-[(2-methylpropan-2-yl)oxy-oxomethyl]-4-(2-methylpropyl)-5-oxazolidinyl]acetic acid
(2'S,3'S,4S)-(-)-(E)-2,2-Dimethyl-3-N-(tert-butoxycarbonyl)-4-[3'-(1'-hydroxy-2',3'-epoxypropyl)oxazolidine
(R)-4-((2R,3R)-3-Hydroxymethyl-oxiranyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
1,1-DIMETHYLETHYL-[S-(R*,S*)]-4-(2,5-DIHYDRO-5-OXO-2-FURANYL)-2,2-DIMETHYL-3-OXAZOLIDINECARBOXYLATE
(4S)-2,2-dimethyl-4-[(2S,3R)-3-vinyloxiran-2-yl]oxazolidine-3-carboxylic acid tert-butyl ester
tert-Butyl (4R)-4-(3-benzo[d][1,3]dioxol-5-yl-3-hydroxy-1-propynyl)-2,2-dimethyl-1,3-oxazolane-3-carboxylate
tert-Butyl (4S,4'R)-2,2-dimethyl-4-(4'-ethoxycarbonyl-2'-chloro-3',3'-difluoropent-1'-enyl)oxazolidine-3-carboxylate
(2S,3S)-2-[[tert-butyl(dimethyl)silyl]oxymethyl]-3-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]-5-oxo-1-pyrrolidinecarboxylic acid tert-butyl ester
tert-Butyl (4R)-4-(3-benzo[d][1,3]ioxol-5-yl-3-oxo-1-propynyl)-2,2-dimethyl-1,3-oxazolane-3-carboxylate
(S)-N-(TERT.-BUTOXYCARBONYL)-4-[(METHYLENEDIPHENYLPHOSPHINO)-SULFIDE]-2,2-DIMETHYLOXAZOLIDINE
| Title | Journal or Book | Year |
|---|---|---|
| Syntheses of L-Glutamic Acid Analogues for Neuroexcitatory Activity Studies | Journal of the Chinese Chemical Society | 2000 |
This compound is available in the following databases:
KnowItAll Mass Spectral Library
Author: Wiley
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Wiley Registry of Mass Spectral Data 2023
Author: Wiley
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