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1,1-Dimethylethyl[S-(R(*),S(*)]-4-(1-Hydroxy-4,4-dimethoxy-2-butynyl)-2,2-dimethyl-3-oxazolidinecarboxylate

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

1,1-Dimethylethyl[S-(R(*),S(*)]-4-(1-Hydroxy-4,4-dimethoxy-2-butynyl)-2,2-dimethyl-3-oxazolidinecarboxylate
SpectraBase Compound ID 7da7OjVWrf1
InChI InChI=1S/C16H27NO6/c1-15(2,3)23-14(19)17-11(10-22-16(17,4)5)12(18)8-9-13(20-6)21-7/h11-13,18H,10H2,1-7H3/t11-,12-/m0/s1
InChIKey JXWOATDMQDKKBC-RYUDHWBXSA-N
Mol Weight 329.39 g/mol
Molecular Formula C16H27NO6
Exact Mass 329.183838 g/mol
Enantiomer InChIKey JXWOATDMQDKKBC-VXGBXAGGSA-N

View Spectrum of 1,1-Dimethylethyl[S-(R(*),S(*)]-4-(1-Hydroxy-4,4-dimethoxy-2-butynyl)-2,2-dimethyl-3-oxazolidinecarboxylate

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-55-3779-6

View Spectrum of 1,1-Dimethylethyl[S-(R(*),S(*)]-4-(1-Hydroxy-4,4-dimethoxy-2-butynyl)-2,2-dimethyl-3-oxazolidinecarboxylate

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-55-3779-7

View Spectrum of 1,1-Dimethylethyl[S-(R(*),S(*)]-4-(1-Hydroxy-4,4-dimethoxy-2-butynyl)-2,2-dimethyl-3-oxazolidinecarboxylate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
tert-Butyl 4-(1-hydroxyhexadecyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate
(4S,1'R)-3-(tert-Butyloxycarbonyl)-2,2-dimethyl-4-(1'-hydroxypent-4-enyl)-1,3-oxazolidine
(R)-4-((E)-(S)-1-Hydroxy-3-methoxymethoxy-allyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
Anti-tert-butyl 4-(1-hydroxynon-2-enyl)-2,2-dimethyloxazolidine-3-carboxylate
(1R,4S)-4-(1-Hydroxyoct-2-enyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester; O,N-Isopropylidene-N-(tert-butoxycarbonyl)-C10-derythro-spinidene
3-Oxazolidinecarboxylic acid, 4-(1-hydroxy-4,4-dimethoxy-2-butenyl)-2,2-dimethyl-, 1,1-dimethylethyl ester, [S-[R*,S*-(Z)]]-
tert-Butyl (4S,1R,2'E)-4-(1'-Hydroxyhexadec-2'-enyl)-2,2-dimethyl-3-oxazolinecarboxylate
(4S)-2,2-dimethyl-4-(1-oxopent-4-enyl)-3-oxazolidinecarboxylic acid tert-butyl ester
(4S,3'RS)-(3'-ETHOXY-3'-PHENYLPROPYL)-2,2-DIMETHYL-OXAZOLIDINE-3-CARBOXYLIC-ACID-TERT.-BUTYLESTER
(4R)-2,2-Dimethyl-4-[(E)-1-methylbuta-1,3-dienyl]oxazolidine-3-carboxylic acid t-butyl ester
Title Journal or Book Year
Glycosyl .alpha.-amino acids via stereocontrolled buildup of a penaldic acid equivalent. A novel synthetic approach to the nucleosidic component of the polyoxins and related substances The Journal of Organic Chemistry 1990
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