(2E,4S)-4-[N-BENZYL-N-[(2E)-(4-HYDROXY-3-METHYL)-2-BUTENYL]-AMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-PENTENOIC-ACID-ETHYLESTER
Compound with spectra: 1 NMR
![(2E,4S)-4-[N-BENZYL-N-[(2E)-(4-HYDROXY-3-METHYL)-2-BUTENYL]-AMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-PENTENOIC-ACID-ETHYLESTER](/api/compound/ArFLR78EDH1.png?ph=true&h=300&w=458 "(2E,4S)-4-[N-BENZYL-N-[(2E)-(4-HYDROXY-3-METHYL)-2-BUTENYL]-AMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-PENTENOIC-ACID-ETHYLESTER")
| SpectraBase Compound ID | ArFLR78EDH1 |
|---|---|
| InChI | InChI=1S/C25H41NO4Si/c1-8-29-24(28)15-14-23(20-30-31(6,7)25(3,4)5)26(17-16-21(2)19-27)18-22-12-10-9-11-13-22/h9-16,23,27H,8,17-20H2,1-7H3/b15-14+,21-16+/t23-/m0/s1 |
| InChIKey | PQXBXLZGYHUQIN-QCLJARCVSA-N |
| Mol Weight | 447.7 g/mol |
| Molecular Formula | C25H41NO4Si |
| Exact Mass | 447.280485 g/mol |
| Enantiomer InChIKey | PQXBXLZGYHUQIN-WVMUXPBLSA-N |
| Racemate InChIKey | PQXBXLZGYHUQIN-OUALVRHLSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2E,4S)-4-[N-BENZYL-N-[(2E)-(4-CHLORO-3-METHYL)-2-BUTENYL]-AMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-PENTENOIC-ACID-ETHYLESTER
N-METHYLAMIDE-DERIVATIVE
(+)-Ethyl 3-[(2S)-1-Benzyl-4-(2,2-dimethoxyethyl)piperazin-2-yl]prop-2-enoate
N,N-Dibenzyl-O-(tert-butyldimethylsilyl)-L-serine benzyl ester
(2S,3R,4E)-2-(N,N-Dibenzylamino)-1-O-(tert-butyldimethylsilyl)-4-octadecene-1,3-diol
(6R/S)-1-Benzyl-6-ethoxycarbonyl-4-methyl-3,4-didehydropiperidine
(S)-5-(TERT.-BUTYLDIMETHYLSILOXYMETHYL)-1-(4-METHOXYPHENYLMETHYL)-2-PYRROLIDINONE
RHQJKDKTQGQDOL-QUWDGAPNSA-N
(2S,4S)-(N-BENZYL)-4-(TERT.-BUTYLDIMETHYLSILYLOXY)-PROLINOL
| Title | Journal or Book | Year |
|---|---|---|
| Total Synthesis of (−)-α-Kainic Acid by (−)-Sparteine-Mediated Asymmetric Deprotonation−Cycloalkylation | Organic Letters | 2004 |