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(2S,4S,5R)-2-[(1'S)-1',2'-DIHYDROXYETHYL]-4-METHYL-5-PHENYL-3-PARA-TOLYLSULFONYLOXAZOLIDINE;SYN-ISOMER

Compound with spectra: 1 NMR, and 2 MS (GC)

(2S,4S,5R)-2-[(1'S)-1',2'-DIHYDROXYETHYL]-4-METHYL-5-PHENYL-3-PARA-TOLYLSULFONYLOXAZOLIDINE;SYN-ISOMER
SpectraBase Compound ID BrHXKI6bFZr
InChI InChI=1S/C19H23NO5S/c1-13-8-10-16(11-9-13)26(23,24)20-14(2)18(15-6-4-3-5-7-15)25-19(20)17(22)12-21/h3-11,14,17-19,21-22H,12H2,1-2H3/t14-,17-,18-,19-/m0/s1
InChIKey HRZGEHPDKKEVNQ-QZHFEQFPSA-N
Mol Weight 377.46 g/mol
Molecular Formula C19H23NO5S
Exact Mass 377.129694 g/mol
Enantiomer InChIKey HRZGEHPDKKEVNQ-UTRMSSBJSA-N

View Spectrum of (2S,4S,5R)-2-[(1'S)-1',2'-DIHYDROXYETHYL]-4-METHYL-5-PHENYL-3-PARA-TOLYLSULFONYLOXAZOLIDINE;SYN-ISOMER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-0-1102-30

View Spectrum of (2S,4S,5R)-2-[(1'S)-1',2'-DIHYDROXYETHYL]-4-METHYL-5-PHENYL-3-PARA-TOLYLSULFONYLOXAZOLIDINE;SYN-ISOMER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QC-7-3437-15

View Spectrum of (2S,4S,5R)-2-[(1'S)-1',2'-DIHYDROXYETHYL]-4-METHYL-5-PHENYL-3-PARA-TOLYLSULFONYLOXAZOLIDINE;SYN-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1R)-1-[(2S,4S,5R)-4-methyl-3-(4-methylphenyl)sulfonyl-5-phenyl-1,3-oxazolidin-2-yl]ethane-1,2-diol
(2S,4S,5R)-2-[(1'R)-1',2'-DIHYDROXYETHYL]-4-METHYL-5-PHENYL-3-PARA-TOLYLSULFONYLOXAZOLIDINE;ANTI-ISOMER
8-[(p-Methylphenyl)sulfonyl]-6-oxa-8-azabicyclo[3.2.1]oct-3-en-2-yl acetate
2H-1,2-benzothiazin-4-ol, 3-[[4-(dimethylamino)phenyl]methyl]-3,4-dihydro-2-(1-methylethyl)-, 1,1-dioxide
trans-N-p-Toluenesulfonyl-5-ethyl-4-(1-allyl-2,2-dimethylvinyl)-2-oxazolidinone
(2S,3R)-5-Benzyl-3-iodo-2-phenyl-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-pyrrole
4-[(E)-1,2-dimethylenepent-3-enyl]-5-methyl-3-(p-tolylsulfonyl)oxazolidin-2-one
N-[(2S,3S,4S,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-iodo-tetrahydropyran-2-yl]-4-nitro-benzenesulfonamide
3-Methyl-6-(3,4-dimethyl-5-phenyl-1,3-oxazolidin-2-yl)-3,4,5,6-tetrahydro-1,2-oxazine
Trimethyl-[(E)-2-[(2S,3S)-1-(4-methylphenyl)sulfonyl-3-(1-naphthalenyl)-2-aziridinyl]ethenyl]silane
2-(3-Pyridyl)-7-(p-toluenesulfonyl)-7-azabicyclo[2.2.1]hept-2-ene
Title Journal or Book Year
An efficient protocol for Sharpless-style racemic dihydroxylation Journal of the Chemical Society, Perkin Transactions 1 1999
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