WWNUHXYWYGAGQG-BMGNFLSWSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 22IzWa1N3Ba |
|---|---|
| InChI | InChI=1S/C21H37NO4Si/c1-9-22(10-2)18(23)17-16-21(17,19(24)25-11-3)14-12-13-15-26-27(7,8)20(4,5)6/h12-15,17H,9-11,16H2,1-8H3/b14-12-,15-13+/t17-,21-/m1/s1 |
| InChIKey | WWNUHXYWYGAGQG-BMGNFLSWSA-N |
| Mol Weight | 395.6 g/mol |
| Molecular Formula | C21H37NO4Si |
| Exact Mass | 395.249185 g/mol |
| Enantiomer InChIKey | WWNUHXYWYGAGQG-BLUCETASSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Dimethyl 2-[2-Hydroxy-2-phenyl-1-(piperidin-1-ylcarbonyl)ethyl]propanedioate
Diethyl 2-(trans-4-(bromomethyl)-1-propyl-2-oxopyrrolidin-3-yl)malonate
(1S,5S,6S)-Methyl 6-[2'-(Z)-styryl]-2-oxabicyclo[3.1.0]hexane-6-carboxylate
Dimethyl 2-[2-Hydroxy-2-phenyl-1-(pyrrolidin-1-ylcarbonyl)ethyl]propanedioate
(E)-(3R,4R)-3-Benzyloxy-1-methyl-2-oxo-2,3,4,7,8,9-hexahydro-1H-azonine-4-carboxylic acid ethyl ester
(E)-(3S,4R)-3-Benzyloxy-1-methyl-2-oxo-2,3,4,7,8,9-hexahydro-1H-azonine-4-carboxylic acid ethyl ester
Di-t-butyl 2-[1-p-nitrophenyl-2-(cyclohexylamino)-2-oxoethyl]malonata
2-keto-1,3,4,5,6,7-hexahydro-1,8-naphthyridine-4a-carboxylic acid ethyl ester
syn-Methyl 4-(tert-morpholinylcarbonyl)-2-phenyl-4-methylhex-4-enoate
(S)-N-[(1S,2S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-2-phenyl-ethyl]-3-dibenzylamino-N-methyl-butyramide
| Title | Journal or Book | Year |
|---|---|---|
| Epoxysilane Rearrangement Induced by a Carbanion Generated by Conjugate Addition of Enolates of Chloroacetate and α-Chloroacetamides: Formation of Functionalized Cyclopropane Derivatives | Organic Letters | 2006 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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