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METHYL-(2S,3R,4R)-4-[(TERT.-BUTOXYCARBONYL)-AMINO]-2-FLUORO-3,5-DIHYDROXYPENTANOATE

Compound with spectra: 2 NMR

METHYL-(2S,3R,4R)-4-[(TERT.-BUTOXYCARBONYL)-AMINO]-2-FLUORO-3,5-DIHYDROXYPENTANOATE
SpectraBase Compound ID 8kLZYEH6dB3
InChI InChI=1S/C11H20FNO6/c1-11(2,3)19-10(17)13-6(5-14)8(15)7(12)9(16)18-4/h6-8,14-15H,5H2,1-4H3,(H,13,17)/t6-,7+,8-/m1/s1
InChIKey HSSVFKDYRNGAMJ-GJMOJQLCSA-N
Mol Weight 281.28 g/mol
Molecular Formula C11H20FNO6
Exact Mass 281.127466 g/mol
Enantiomer InChIKey HSSVFKDYRNGAMJ-RNJXMRFFSA-N

View Spectrum of METHYL-(2S,3R,4R)-4-[(TERT.-BUTOXYCARBONYL)-AMINO]-2-FLUORO-3,5-DIHYDROXYPENTANOATE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of METHYL-(2S,3R,4R)-4-[(TERT.-BUTOXYCARBONYL)-AMINO]-2-FLUORO-3,5-DIHYDROXYPENTANOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
METHYL-(2S,3R,4S)-4-[(TERT.-BUTOXYCARBONYL)-AMINO]-2-FLUORO-3,5-DIHYDROXYPENTANOATE
(3R,4R,5R)-BOC-D-ALLO-ISOSTATIN-ETHYLESTER
ALPHA-METHYL-GAMMA-BENZYL-(2R)-N-(TERT.-BUTOXYCARBONYL)-GLUTAMATE
3-[(1-tert-Butoxycarbonylamido)-3-methylbutyl]oxirane-2-methol
(R/s)-3-Heptanol, 2-(s)-[(tert.butyloxycarbonyl)amino]-1-phenyl-
Boc-D-Glu-OBzl
3-(s)-Pentanol, 2-(R)-[(tert.butyloxycarbonyl)amino]-4,4-dimethyl-1-phenyl-
L-THREONINE, N-[(1,1-DIMETHYLETHOXY)CARBONYL]-, PHENYLMETHYL ESTER
1-Pentanol, 2-[(tert.butyloxycarbonyl)amino]-4-methyl-1-phenyl-, (R or S)
(2S,3S)-N-(tert-Butoxycarbonyl)-3-amino-5-methyl-1-[(4-methylphenyl)sulfenyl]-2-hexanol
Title Journal or Book Year
Synthetic Routes towards Fluorine-Containing Amino Sugars: Synthesis of Fluorinated Analogues of Tomosamine and 4-Amino-4-deoxyarabinose European Journal of Organic Chemistry 2014
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