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(2'R,2''S,3''S,4R,5S,5''R)-(+)-3-[2'-(3'',5''-DIMETHYL-6''-OXOTETRAHYDROPYRAN-2''-YL)-1'-OXOBUTYL]-4-METHYL-5-PHENYLOXAZOLIDIN-2-ONE

Compound with spectra: 1 NMR

(2'R,2''S,3''S,4R,5S,5''R)-(+)-3-[2'-(3'',5''-DIMETHYL-6''-OXOTETRAHYDROPYRAN-2''-YL)-1'-OXOBUTYL]-4-METHYL-5-PHENYLOXAZOLIDIN-2-ONE
SpectraBase Compound ID C4OPxDRfXni
InChI InChI=1S/C21H27NO5/c1-5-16(17-12(2)11-13(3)20(24)26-17)19(23)22-14(4)18(27-21(22)25)15-9-7-6-8-10-15/h6-10,12-14,16-18H,5,11H2,1-4H3/t12-,13+,14-,16+,17?,18-/m1/s1
InChIKey GOQDGZIBRATNHJ-BGPMTTNMSA-N
Mol Weight 373.45 g/mol
Molecular Formula C21H27NO5
Exact Mass 373.188923 g/mol
Enantiomer InChIKey GOQDGZIBRATNHJ-IDZHFINDSA-N

View Spectrum of (2'R,2''S,3''S,4R,5S,5''R)-(+)-3-[2'-(3'',5''-DIMETHYL-6''-OXOTETRAHYDROPYRAN-2''-YL)-1'-OXOBUTYL]-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
2-Oxazolidinone, 4-methyl-3-[1-oxo-2-(tetrahydro-3,5-dimethyl-6-oxo-2H-pyran-2-yl)butyl]-5-phenyl-, [2S-[2.alpha.[S*(4S*,5R*)],3.beta.,5.beta.]]-
2-Oxazolidinone, 3-[7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-ethyl-4,6-dimethyl-1-oxo-3-[(trimethylsilyl)oxy]heptyl]-4-methyl-5-phenyl-, [4R-[3(2R*,3S*,4S*,6R*),4.alpha.,5.alpha.]]-
(4R,5S)-4-Methyl-3-[(2R,3R)-2-methyl-3-phenyl-3-(tosylamino)propionyl]-5-phenyloxazolodin-2-one
(+)-(4R,5S)-3-{(2R.3S)-(E)-6-(2-Bromo-1-cyclohexanylidene)-5,5-(ethylidenedioxy)-3-hydroxy-2-methylhexanoyl}-4-methyl-5-phenyl-2-oxazolidinone
(4R,5S)-3-[1-Oxo-3-(1,3-dithian-2-ylidene)-2-[3,4-(methylenedioxy)benzyl]propyl]-4-methyl-5-phenyl-2-oxazolidenone
(4S,5R)-4-Methyl-3-[(2R,3R)-2-methyl-3-phenyl-3-(tosylamino)propionyl)-5-phenyloxazolidin-2-one
(4R,5S)-4-Methyl-3-[(2R,3S)-2-methyl-3-phenyl-3-(tosylamino)propionyl]-5-phenyloxazolodin-2-one
(4S,5R)-4-Methyl-3-[(2R,3S)-2-methyl-3-phenyl-3-(tosylamino)propionyl)-5-phenyloxazolidin-2-one
LSPBZOJZFSBHBQ-LUXFFAPCSA-N
3-Phenyl-5-phenylthio-2-[(4-tert-butyl-2-oxotetrahydro[1,3]oxazol)carbonyl]cyclohexanol
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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