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(2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANALDEHYDE;MAJOR-ISOMER

Compound with spectra: 2 NMR

(2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANALDEHYDE;MAJOR-ISOMER
SpectraBase Compound ID 2J0RAdHF0R1
InChI InChI=1S/C20H35NO3Si2/c1-20(2,3)26(7,8)24-15-18(14-22)21(16-25(4,5)6)19(23)17-12-10-9-11-13-17/h9-14,18H,15-16H2,1-8H3/t18-/m0/s1
InChIKey ZJBLSAUWACURAW-SFHVURJKSA-N
Mol Weight 393.7 g/mol
Molecular Formula C20H35NO3Si2
Exact Mass 393.215547 g/mol
Enantiomer InChIKey ZJBLSAUWACURAW-GOSISDBHSA-N
Racemate InChIKey ZJBLSAUWACURAW-UHFFFAOYSA-N

View Spectrum of (2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANALDEHYDE;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANALDEHYDE;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (2S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-1-PROPANALDEHYDE;MINOR-ISOMER
(2S)-3-(tert-Butyldimethylsiloxy)-2-[N-[(trimethylsilyl)methyl]-N-benzoylamino]-1-propanal
(3R,4S)-1-(TRIMETHYLSILYL)-3-HYDROXY-4-[N-BENZOYL-N-[(TRIMETHYLSILYL)-METHYL]-AMINO]-1-(E)-PENTENE
N-[(E,1S,2R)-2-hydroxy-1-methyl-4-trimethylsilyl-but-3-enyl]-N-(trimethylsilylmethyl)benzamide
ACETAMIDE-DERIVATIVE
ETHYL-N-BENZOYL-S-PROLYLOATE
(2E,4S)-4-[BENZYL-[(2E)-4-CHLORO-3-METHYL-2-BUTENYL]-AMINO]-5-[[TERT.-BUTYL-(DIMETHYL)-SILYL]-OXY]-2-PENTENYL-DIISOPROPYLCARBAMATE
(2E,4S)-4-[N-BENZYL-N-[(2E)-(4-CHLORO-3-METHYL)-2-BUTENYL]-AMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-PENTEN-1-YL-N,N-DIISOPROPYLCARBAMATE
2-[benzoyl(isopropyl)amino]-3-phenyl-propanoic acid
N-Benzoyl-2-[(benzoyloxy)methyl]piperidine
N-[3,4-DIMETHOXYBENZYL]-N-[TRIMETHYLSILYLMETHYL]-BENZAMIDE
Title Journal or Book Year
An Oxidative Mannich Cyclization Methodology for the Stereocontrolled Synthesis of Highly Functionalized Piperidines The Journal of Organic Chemistry 1998
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