(+/-)-N-TERT.-BUTYL-2-HYDROXY-2-CYCLOHEXYLACETYLAMIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Gy0uxfu78xh |
|---|---|
| InChI | InChI=1S/C12H23NO2/c1-12(2,3)13-11(15)10(14)9-7-5-4-6-8-9/h9-10,14H,4-8H2,1-3H3,(H,13,15) |
| InChIKey | FBKIGMDJQCSGFH-UHFFFAOYSA-N |
| Mol Weight | 213.32 g/mol |
| Molecular Formula | C12H23NO2 |
| Exact Mass | 213.172879 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
cyclohexyl(hydroxymethyl) pentyl ketone
(+/-)-N-TERT.-BUTYL-2-HYDROXY-4-PHENYLBUTAMIDE
(S)-iso-Propyl-2-cyclohexyl-2-hydroxyacetate
ALPHA-HYDROXY-ALPHA-(1-FLUOROCYCLOHEXYL)ACETAMIDE
(3R)-N-tert-butyl-3-methyl-5-phenyl-valeramide
(R)-N-tert-Butyl-3-methyl-5-phenyl-pentanamide
(1S,2S)-N-METHYL-1-CYCLOHEXYL-1-METHOXYPROP-2-YL-AMINE
(1R,2S)-N-METHYL-1-CYCLOHEXYL-1-METHOXYPROP-2-YL-AMINE
2-Hydroxyhexacosanoic Acid - Pyrrolidide
2-Hydroxyheptacosanoic Acid - Pyrrolidide
| 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 |