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(S(S),3S)-ETHYL-N-(PARA-TOLYLSULFINYL)-3-AMINO-2,2-DIFLUORO-3-PHENYLPROPANOATE

Compound with spectra: 3 NMR

(S(S),3S)-ETHYL-N-(PARA-TOLYLSULFINYL)-3-AMINO-2,2-DIFLUORO-3-PHENYLPROPANOATE
SpectraBase Compound ID EdtxvMtLvGL
InChI InChI=1S/C18H19F2NO3S/c1-3-24-17(22)18(19,20)16(14-7-5-4-6-8-14)21-25(23)15-11-9-13(2)10-12-15/h4-12,16,21H,3H2,1-2H3/t16-,25?/m1/s1
InChIKey JCXCOFQNEFZPQI-ZRTDVJLTSA-N
Mol Weight 367.41 g/mol
Molecular Formula C18H19F2NO3S
Exact Mass 367.105371 g/mol
Enantiomer InChIKey JCXCOFQNEFZPQI-YPHZTSLFSA-N

View Spectrum of (S(S),3S)-ETHYL-N-(PARA-TOLYLSULFINYL)-3-AMINO-2,2-DIFLUORO-3-PHENYLPROPANOATE

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

View Spectrum of (S(S),3S)-ETHYL-N-(PARA-TOLYLSULFINYL)-3-AMINO-2,2-DIFLUORO-3-PHENYLPROPANOATE

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

View Spectrum of (S(S),3S)-ETHYL-N-(PARA-TOLYLSULFINYL)-3-AMINO-2,2-DIFLUORO-3-PHENYLPROPANOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (R(S),3R)-ETHYL-N-(PARA-TOLYLSULFINYL)-3-AMINO-2,2-DIFLUORO-3-PHENYLPROPANOATE
Methyl 2-[(4-Chlorophenyl)(toluene-4-sulfonylamino)methyl]acrylate
(S)-tert-Butyl N-(2-(phenoxycarbonyl)-2,2-difluoro-1-phenylethyl)carbamate
(2R,3R)-2-amino-3-phenyl-3-(tosylamino)propionic acid ethyl ester
Ethyl (2R,3R)-2-amino-3-(N-tosylamino)-3-(4-iodophenyl)propionate
trans-Methyl 2-hydroxy-3-(p-fluoro)phenyl-3'-(N-tosylamino)propanoate
cis-Methyl 2-hydroxy-3-(p-fluoro)phenyl-3'-(N-tosylamino)propanoate
(2S,3R)-3-(4-chlorophenyl)-2-hydroxy-3-(tosylamino)propionic acid methyl ester
(2R,3R)-3-(4-chlorophenyl)-2-hydroxy-3-(tosylamino)propionic acid methyl ester
cis-Methyl 2-hydroxy-3-(p-methoxy)phenyl-3'-(N-tosylamino)propanoate
cis-Methyl 2-hydroxy-3-(p-methyl)phenyl-3'-(N-tosylamino)propanoate
Title Journal or Book Year
Convenient Asymmetric Synthesis of β-Substituted α,α-Difluoro-β-amino Acids via Reformatsky Reaction between Davis' N-Sulfinylimines and Ethyl Bromodifluoroacetate The Journal of Organic Chemistry 2003

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