(-)-N-(TOSYLMETHYL)-2-HYDROXY-4-PHENYLBUTAMIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 2fZ5YRkJiK1 |
|---|---|
| InChI | InChI=1S/C16H17NO4S/c1-12-7-9-14(10-8-12)22(20,21)11-17-16(19)15(18)13-5-3-2-4-6-13/h2-10,15,18H,11H2,1H3,(H,17,19) |
| InChIKey | BZHXWTRIGAJJDI-UHFFFAOYSA-N |
| Mol Weight | 319.38 g/mol |
| Molecular Formula | C16H17NO4S |
| Exact Mass | 319.087829 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2-((4-bromophenyl)(methyl)amino)-N-(tosylmethyl)acetamide
N-(Tosyldeuteriomethyl)-2,2-dimethylpropanamide
1-Phenyl-3-(p-tolylsulfonylmethyl)but-3-en-1-ol
(S)-(+)-N-Benzyl-2-hydroxy-2-(3'-chlorophenyl)acetamide
N-[3-(ethylanilino)propyl]-3-[(4-methylphenyl)sulfonyl]propanamide
1-[[3-ethyl-2-(2-propenyloxy)-2-pentenyl]sulfonyl]-4-methylbenzene
2-Hydroxy-N'-[(E)-(2-hydroxy-4-methylphenyl)methylidene]-2-phenylacetohydrazide
Benzene, 1-methyl-4-[[3-methyl-2-(phenylmethoxy)-2-butenyl]sulfonyl]-
2-(p-tolylsulfonylmethyl)aniline
1-Phenylthio-2-methyl-3-tosyl-2-propanol
| 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 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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