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(3S,4R)-1-(TRIMETHYLSILYL)-4-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-(E)-PENTEN-3-OL

Compound with spectra: 1 NMR, and 1 MS (GC)

(3S,4R)-1-(TRIMETHYLSILYL)-4-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-(E)-PENTEN-3-OL
SpectraBase Compound ID BDqbBThvvjR
InChI InChI=1S/C25H47NO3Si3/c1-25(2,3)32(10,11)29-19-22(23(27)17-18-30(4,5)6)26(20-31(7,8)9)24(28)21-15-13-12-14-16-21/h12-18,22-23,27H,19-20H2,1-11H3/b18-17+/t22-,23-/m1/s1
InChIKey KCDMINRNFVESTJ-GERLKTCDSA-N
Mol Weight 493.9 g/mol
Molecular Formula C25H47NO3Si3
Exact Mass 493.286374 g/mol
Enantiomer InChIKey KCDMINRNFVESTJ-ZRPIXQTESA-N

View Spectrum of (3S,4R)-1-(TRIMETHYLSILYL)-4-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-(E)-PENTEN-3-OL

MS (GC) Spectrum
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Source of Spectrum J-63-858-79

View Spectrum of (3S,4R)-1-(TRIMETHYLSILYL)-4-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-(E)-PENTEN-3-OL

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (3R,4R)-1-(Trimethylsilyl)-4-[N-[(trimethylsilyl)methyl]-N-benzoylamino]-5-(tert-butyldimethylsioxy)-1(E)-propen-3-ol
  • N-[(E,2R,3R)-1-[tert-butyl(dimethyl)silyl]oxy-3-hydroxy-5-trimethylsilylpent-4-en-2-yl]-N-(trimethylsilylmethyl)benzamide
  • N-[(E,2R,3R)-1-[tert-butyl(dimethyl)silyl]oxy-3-oxidanyl-5-trimethylsilyl-pent-4-en-2-yl]-N-(trimethylsilylmethyl)benzamide
(3R,4R)-1-(TRIMETHYLSILYL)-4-[N-[(TRIMETHYLSILYL)-METHYL]-N-BENZOYLAMINO]-5-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-(E)-PENTEN-3-OL
JSHOWCPHLJJEBQ-HZPDHXFCSA-N
(3S,4S)-1-Benzyl-3,4-bis-(tert-butyl-dimethyl-silanyloxymethyl)-azetidin-2-one
1-(2-Chlorobenzoyl)proline, tms derivative
4a(2H)-Quinolinol, 1-benzoyloctahydro-, trans-
4a(2H)-Quinolinol, 1-benzoyloctahydro-, cis-
(4-Hydroxyoctahydroquinolin-1-yl)(phenyl)methanone
Cyclohexan-1-ol-2-amine, N,N,o-tribenzoyl-
2-[(1S,2S)-1,3-bis(oxidanyl)-1-phenyl-propan-2-yl]isoindole-1,3-dione
Benzamide, N-[2-(acetylamino)cyclohexyl]-N-(2-phenylethyl)-, trans-
Benzamide, N-[2-(acetylamino)cyclohexyl]-N-(2-phenylethyl)-, cis-
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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