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(2S,4S,5S)-4-BENZYL-N-(BENZYLOXYCARBONYL)-2-PHENYL-5-(TRIFLUOROMETHYL)-5-[(TRIMETHYLSILYL)-OXY]-1,3-OXAZOLIDINE

Compound with spectra: 2 NMR

(2S,4S,5S)-4-BENZYL-N-(BENZYLOXYCARBONYL)-2-PHENYL-5-(TRIFLUOROMETHYL)-5-[(TRIMETHYLSILYL)-OXY]-1,3-OXAZOLIDINE
SpectraBase Compound ID GjFTPQrxGAH
InChI InChI=1S/C28H30F3NO4Si/c1-37(2,3)36-27(28(29,30)31)24(19-21-13-7-4-8-14-21)32(25(35-27)23-17-11-6-12-18-23)26(33)34-20-22-15-9-5-10-16-22/h4-18,24-25H,19-20H2,1-3H3/t24-,25-,27-/m0/s1
InChIKey MAYIZTDGUDJAHZ-KLJDGLGGSA-N
Mol Weight 529.63 g/mol
Molecular Formula C28H30F3NO4Si
Exact Mass 529.189619 g/mol
Enantiomer InChIKey MAYIZTDGUDJAHZ-RGSZASNESA-N

View Spectrum of (2S,4S,5S)-4-BENZYL-N-(BENZYLOXYCARBONYL)-2-PHENYL-5-(TRIFLUOROMETHYL)-5-[(TRIMETHYLSILYL)-OXY]-1,3-OXAZOLIDINE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (2S,4S,5S)-4-BENZYL-N-(BENZYLOXYCARBONYL)-2-PHENYL-5-(TRIFLUOROMETHYL)-5-[(TRIMETHYLSILYL)-OXY]-1,3-OXAZOLIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S,4S,5S)-4-BENZYL-N-(BENZYLOXYCARBONYL)-2-(4'-METHOXYPHENYL)-5-(TRIFLUOROMETHYL)-5-[(TRIMETHYLSILYL)-OXY]-1,3-OXAZOLIDINE
1H-pyrido[3,4-b]indole-3-carboxylic acid, 1-(2,4-dimethoxyphenyl)-2,3,4,9-tetrahydro-
(6R)-9,10-dimethoxy-3,6-dimethyl-4-phenyl-4,6,7,11b-tetrahydro-1H-pyrimido[6,1-a]isoquinolin-2-one
5-Chloroacetylamino-3-methyl-1-phenyl-1H-thieno[3,2-e]pyrazolo[3,4-b]pyrazine-6-carbonitrile
Ethyl 2-Methyl-6,7-methylenedioxy-1-oxo-4-(3,4,5-trimethoxyphenyl)-1,2,3,4-tetrahydronaphthalene-3-carboxylate
6H-Pyrrolo[3',4':3,4]pyrrolo[2,1-a]isoquinoline-9,11(5H,10H)-dione, 8,8a,11a,11b-tetrahydro-10-methyl-8-phenyl-, (8.alpha.,8a.alpha.,11a.alpha.,11b.beta.)-
(3S*,3aR*,8aR*)-2,2-Dimethyl-2,3,3a,6,7,8a-hexahydro-3-[(triisopropyl)silyloxy]-5-(methoxycarbonyl)-5H-1,8-dioxacyclopenta[a]indene-4-one
2-[2-(2,6-DICHLOROPHENYLAMINO)-PHENYLMETHYL]-3-[4-[(3-CHLOROPHENYL)-AMINO]-1,3-OXAZOL-2-YL]-QUINAZOLIN-4(3H)-ONE
2-CHLORO-3-[(1,2-DIHYDRO-1-ETHYL-3,6,7-TRIMETHYL-2-QUINOXALINYLIDENE)METHYL]-1,4-NAPHTHOQUINONE
Vallapanin
Title Journal or Book Year
Reaction of (Trifluoromethyl)trimethylsilane with Oxazolidin-5-ones:  Synthesis of Peptidic and Nonpeptidic Trifluoromethyl Ketones The Journal of Organic Chemistry 1998
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