(+/-)-N-TERT.-BUTYL-2-HYDROXY-2-(2-FURYL)-ACETAMIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 2itKFR9YHUP |
|---|---|
| InChI | InChI=1S/C10H15NO3/c1-10(2,3)11-9(13)8(12)7-5-4-6-14-7/h4-6,8,12H,1-3H3,(H,11,13) |
| InChIKey | QCSLWLJOMZISRZ-UHFFFAOYSA-N |
| Mol Weight | 197.23 g/mol |
| Molecular Formula | C10H15NO3 |
| Exact Mass | 197.105193 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(+/-)-N-TERT.-BUTYL-2-HYDROXY-2-(4-METHYLPHENYL)-ACETAMIDE
2-(mandeloylamino)acetic acid ethyl ester
2-Hydroxy-2-phenyl-N,N-di(propan-2-yl)acetamide
2-hydroxy-N-(2-morpholin-4-ylethyl)-2-phenylacetamide
2-(3-Methylfuran-2-yl)-N,N-diethylacetamide
(+)-N-Benzyl-(S)-mandelamide
3-Butene-1,2-diol, 1-(2-furanyl)-2-methyl-
1-[2-(2-furanyl)ethyl]pyrrolidine-2,5-dione
cis-2-Amido-3-furylpropanol
Benzamide, 4-fluoro-N-[2-(2-furanyl)ethyl]-
| Title | Journal or Book | Year |
|---|---|---|
| The First Catalytic, Asymmetric α-Additions of Isocyanides. Lewis-Base-Catalyzed, Enantioselective Passerini-Type Reactions | Journal of the American Chemical Society | 2003 |