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(S)-4-BENZYL-2,2,5,5-TETRAMETHYL-3-[(R)-3-PHENYLBUTANOYL]-OXAZOLIDINE

Compound with spectra: 2 NMR

(S)-4-BENZYL-2,2,5,5-TETRAMETHYL-3-[(R)-3-PHENYLBUTANOYL]-OXAZOLIDINE
SpectraBase Compound ID 4nD2ty5oyj0
InChI InChI=1S/C24H31NO2/c1-18(20-14-10-7-11-15-20)16-22(26)25-21(17-19-12-8-6-9-13-19)23(2,3)27-24(25,4)5/h6-15,18,21H,16-17H2,1-5H3/t18?,21-/m0/s1
InChIKey YAZHIBDMCVXQBG-ZYZRXSCRSA-N
Mol Weight 365.52 g/mol
Molecular Formula C24H31NO2
Exact Mass 365.235479 g/mol
Enantiomer InChIKey YAZHIBDMCVXQBG-BDPMCISCSA-N

View Spectrum of (S)-4-BENZYL-2,2,5,5-TETRAMETHYL-3-[(R)-3-PHENYLBUTANOYL]-OXAZOLIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (S)-4-BENZYL-2,2,5,5-TETRAMETHYL-3-[(R)-3-PHENYLBUTANOYL]-OXAZOLIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (S)-4-BENZYL-2,2,5,5-TETRAMETHYL-3-[(S)-3-PHENYLBUTANOYL]-OXAZOLIDINE
(S)-3-Acryloyl-4-benzyl-2,2-diethyl-5,5-dimethyloxazolidine
(S)-4-Benzyl-3-[2-methoxy-3-methyl-4-(methoxycarbonyl)butanoyl]-2,2-dimethyloxazolidine
(4R)-4-BENZYL-3-[(2S,3R)-2-BENZYL-3-HYDROXY-5-PHENYLPENTANOYL]-1,3-OXAZOLIDIN-2-ONE
(4S)-4-Benzyl-3-({[6-(1,4-dioxaspiro[4.5]dec-6-en-7-yl)hex-2-ynyl]dimethylsilyl}methyl)-5,5-dimethyloxazolidin-2-one
N-Benzyl-3,4-dimethyl-2-[(2''-oxo-4''-benzyloxazol-2"-yl)2'-oxoethyl]piperidine
(4S)-4-Benzyl-3-[(2S,3R)-2-methyl-3-(tetrahydro-2H-pyran-2-yloxy)decanoyl]-1,3-oxazolidin-2-one
(R)-3-((S)-Hydroxy-phenyl-methyl)-7a-methyl-2,3-dihydro-7aH-pyrrolo[2,1-b]oxazol-5-one
(4-S)-BENZYL-3-[(2-R,3-S)-3-(4-CHLOROPHENYL)-3-HYDROXY-2-(TRIFLUOROMETHYL)-PROPANOYL]-OXAZOLIDIN-2-ONE
(8S,11R)-11-Methyl-8-{2-oxo-2-[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]ethyl}-7-oxa-1,5-dithiaspiro[5.5]undecane
(4R)-N-[(2S)-2-METHYL-1-OXO-3-PHENYLPROPYL]-5,5-DIMETHYL-4-PHENYLOXAZOLIDIN-2-ONE;MAJOR-DIASTEREOISOMER
Title Journal or Book Year
Effective Enantiocontrol in Conjugate Additions of Organocuprates. Highly Selective 1,5-Chiral Induction in the Conjugate Additions of Cuprates to .alpha.,.beta.-Unsaturated Amide Derivatives of 2,2-Dimethyloxazolidine Chiral Auxiliaries The Journal of Organic Chemistry 1994
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