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(4-S)-BENZYL-3-[(2-S,3-S)-3-HYDROXY-3-(4-METHYLPHENYL)-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE

Compound with spectra: 1 NMR

(4-S)-BENZYL-3-[(2-S,3-S)-3-HYDROXY-3-(4-METHYLPHENYL)-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
SpectraBase Compound ID LccuG9MspLT
InChI InChI=1S/C21H20F3NO4/c1-13-7-9-15(10-8-13)18(26)17(21(22,23)24)19(27)25-16(12-29-20(25)28)11-14-5-3-2-4-6-14/h2-10,16-18,26H,11-12H2,1H3/t16-,17-,18-/m0/s1
InChIKey JDLHGWOHPUMFDB-BZSNNMDCSA-N
Mol Weight 407.39 g/mol
Molecular Formula C21H20F3NO4
Exact Mass 407.134443 g/mol
Enantiomer InChIKey JDLHGWOHPUMFDB-KZNAEPCWSA-N

View Spectrum of (4-S)-BENZYL-3-[(2-S,3-S)-3-HYDROXY-3-(4-METHYLPHENYL)-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE

19F NMR Spectrum
Copyright Copyright © 2016-2024 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-(4-METHYLPHENYL)-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-(4-CHLOROPHENYL)-3-HYDROXY-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
(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-HYDROXY-3-PHENYL-2-(TRIFLUOROMETHYL)-PROPANOYL]-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
3-{(2S,3R,5R) 2'-Allyl-5'-[(t-butyl)dimethylsilyloxy]-3'-hydroxy-7'-octynoyl}-4-benzyl-1,3-oxazolidin-2-one
(4S,2'S,3'S)-3-[2'-Methyl-3'-[(4"-nitrobenzoyl)oxy]-7'-octyoyl]-4-phenymethyl-2-oxazolidinone
(4S)-4-Benzyl-3-[(2S,3R)-2-methyl-3-(tetrahydro-2H-pyran-2-yloxy)decanoyl]-1,3-oxazolidin-2-one
(4S)-3-[(2S,3R,5R)-5-[tert-butyl(dimethyl)silyl]oxy-3-hydroxy-7-[(4-methoxyphenyl)methoxy]-2-methyl-1-oxoheptyl]-4-(phenylmethyl)-2-oxazolidinone
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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