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(4-S)-Benzyl-3-[(2-S,3-S)-3-hydroxy-3-phenyl-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one

Compound with spectra: 2 NMR

(4-S)-Benzyl-3-[(2-S,3-S)-3-hydroxy-3-phenyl-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one
SpectraBase Compound ID KmBp2T6gpz0
InChI InChI=1S/C20H18F3NO4/c21-20(22,23)16(17(25)14-9-5-2-6-10-14)18(26)24-15(12-28-19(24)27)11-13-7-3-1-4-8-13/h1-10,15-17,25H,11-12H2/t15-,16-,17-/m0/s1
InChIKey BACKHYXFAVCRKS-ULQDDVLXSA-N
Mol Weight 393.36 g/mol
Molecular Formula C20H18F3NO4
Exact Mass 393.118793 g/mol
Enantiomer InChIKey BACKHYXFAVCRKS-BRWVUGGUSA-N

View Spectrum of (4-S)-Benzyl-3-[(2-S,3-S)-3-hydroxy-3-phenyl-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one

13C NMR Spectrum
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View Spectrum of (4-S)-Benzyl-3-[(2-S,3-S)-3-hydroxy-3-phenyl-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one

19F NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(4-S)-BENZYL-3-[(2-R,3-S)-3-HYDROXY-3-PHENYL-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
(4-S)-Benzyl-3-[(2-S,3-S)-3-(4-chlorophenyl)-3-hydroxy-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one
(4-S)-BENZYL-3-[(2-R,3-S)-3-(4-CHLOROPHENYL)-3-HYDROXY-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
(4-S)-Benzyl-3-[(2-S,3-S)-3-hydroxy-3-(4-methylphenyl)-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one
(4-S)-BENZYL-3-[(2-R,3-S)-3-HYDROXY-3-(4-METHYLPHENYL)-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
(4-S)-Benzyl-3-[(2-R,3-S)-3-(4-fluorophenyl)-3-hydroxy-2-(trifluoromethyl)-propanoyl]-oxazolidin-2-one
(4R)-4-BENZYL-3-[(2S,3R)-2-BENZYL-3-HYDROXY-5-PHENYLPENTANOYL]-1,3-OXAZOLIDIN-2-ONE
(R)-4-Benzyl-3-{(E)-(2R,3R,6S,7S)-3-hydroxy-7-[(4-methoxybenzyl)oxy]-2,4,6-(trimethyl)oct-4-enoyl}oxazolidin-2-one
(4S)-4-Benzyl-3-[(2S,3R)-2-methyl-3-(tetrahydro-2H-pyran-2-yloxy)decanoyl]-1,3-oxazolidin-2-one
(S)-4-Benzyl-3-{(S)-5-benzyloxymethyl-2-[(R)-1-(2-methoxy-ethoxymethoxy)-ethyl]-hex-5-enoyl}-oxazolidin-2-one
Title Journal or Book Year
Highly Stereoselective TiCl4-Catalyzed Evans−Aldol and Et3Al-Mediated Reformatsky Reactions. Efficient Accesses to Optically Active syn- or anti-α-Trifluoromethyl-β-hydroxy Carboxylic Acid Derivatives Organic Letters 2006
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