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(2'R,3'S,4R,4'S,5S,6'R)-(-)-3-(2'-ETHYL-7'-HYDROXY-4',6'-DIMETHYL-1'-OXO-3'-TRIMETHYLSILYLOXYHEPTYL)-4-METHYL-5-PHENYLOXAZOLIDIN-2-ONE

Compound with spectra: 1 NMR

(2'R,3'S,4R,4'S,5S,6'R)-(-)-3-(2'-ETHYL-7'-HYDROXY-4',6'-DIMETHYL-1'-OXO-3'-TRIMETHYLSILYLOXYHEPTYL)-4-METHYL-5-PHENYLOXAZOLIDIN-2-ONE
SpectraBase Compound ID KVCO9n4GcjX
InChI InChI=1S/C24H39NO5Si/c1-8-20(21(30-31(5,6)7)17(3)14-16(2)15-26)23(27)25-18(4)22(29-24(25)28)19-12-10-9-11-13-19/h9-13,16-18,20-22,26H,8,14-15H2,1-7H3/t16-,17+,18+,20-,21+,22+/m0/s1
InChIKey SXADSKZCXNBDKK-CJBPLUAASA-N
Mol Weight 449.7 g/mol
Molecular Formula C24H39NO5Si
Exact Mass 449.25975 g/mol
Enantiomer InChIKey SXADSKZCXNBDKK-NWUMPJBXSA-N

View Spectrum of (2'R,3'S,4R,4'S,5S,6'R)-(-)-3-(2'-ETHYL-7'-HYDROXY-4',6'-DIMETHYL-1'-OXO-3'-TRIMETHYLSILYLOXYHEPTYL)-4-METHYL-5-PHENYLOXAZOLIDIN-2-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(4R,5S)-3-[(2R,3S,4S,6R)-2-ethyl-4,6-dimethyl-7-oxidanyl-3-trimethylsilyloxy-heptanoyl]-4-methyl-5-phenyl-1,3-oxazolidin-2-one
2-Oxazolidinone, 3-[2-ethyl-4,6-dimethyl-1-oxo-3-[(trimethylsilyl)oxy]-6-heptenyl]-4-methyl-5-phenyl-, [4R-[3(2R*,3S*,4S*),4.alpha.,5.alpha.]]-
(4S,5S)-3-(Bicyclo(4.4.0)dec-2-ene-5-carbonyl)-4-methyl-5-phenyl-2-oxazolidinone
(4S,5S)-3-(Bicyclo(4.3.0)non-2-ene-5-carbonyl)-4-methyl-5-phenyl-2-oxazolidinone
2-Oxazolidinone, 3-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5-iodo-2,4-dimethyl-1-oxo-4-pentenyl]-4-methyl-5-phenyl-, [4R-[3(2R*,3R*,4E),4.alpha.,5.alpha.]]-
(4R,5S,6'R)-(1',4'-Dioxaspiro[4.5]decane-6'-carbonyl)-4-methyl-5-phenyloxazolidin-2-one
YQCSAXABGCMYNR-ANPQRQHMSA-N
(2'R,3'S,5'S,4R,5S)-3-(3'-Hydroxy-5',6'-(isopropylidenedioxy)-2'-(methylthio)hexanoyl)-4-methyl-5-phenyl-2-oxazolidinone
(4S,5R)-3-[3-[(4R,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-2,2,5-trimethyl-1,3-dioxolan-4-yl]-1-oxopropyl]-4-methyl-5-phenyl-2-oxazolidinone
(+-)-(4S,5R)-3-[(1R,2R)-2-Cyclohexylcyclopropyl]-4,5-diphenyloxazolidin-2-one
Title Journal or Book Year
Stereocontrolled Synthesis of a Key Lactone Intermediate Required for the Synthesis of Salinomycin Australian Journal of Chemistry 1990

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