For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

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

Compound with spectra: 1 NMR

(4-S)-BENZYL-3-[(2-S,3-S)-3-(4-CHLOROPHENYL)-3-HYDROXY-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
SpectraBase Compound ID KaDB5zYJqDI
InChI InChI=1S/C20H17ClF3NO4/c21-14-8-6-13(7-9-14)17(26)16(20(22,23)24)18(27)25-15(11-29-19(25)28)10-12-4-2-1-3-5-12/h1-9,15-17,26H,10-11H2/t15-,16-,17-/m0/s1
InChIKey MDJFAFLKVPEOSF-ULQDDVLXSA-N
Mol Weight 427.81 g/mol
Molecular Formula C20H17ClF3NO4
Exact Mass 427.07982 g/mol
Enantiomer InChIKey MDJFAFLKVPEOSF-BRWVUGGUSA-N

View Spectrum of (4-S)-BENZYL-3-[(2-S,3-S)-3-(4-CHLOROPHENYL)-3-HYDROXY-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-(4-CHLOROPHENYL)-3-HYDROXY-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-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-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
(4S,2'S,3'S)-3-[2'-Methyl-3'-[(4"-nitrobenzoyl)oxy]-7'-octyoyl]-4-phenymethyl-2-oxazolidinone
3-{(2S,3R,5R) 2'-Allyl-5'-[(t-butyl)dimethylsilyloxy]-3'-hydroxy-7'-octynoyl}-4-benzyl-1,3-oxazolidin-2-one
(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
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.