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ETHYL-(4S,3'S)-2-OXO-3-(9-PHENYLFLUOREN-9-YL)-OXAZOLIDINE-4-(2',2'-DIFLUORO-3'-HYDROXY)-PROPANOATE

Compound with spectra: 2 NMR

ETHYL-(4S,3'S)-2-OXO-3-(9-PHENYLFLUOREN-9-YL)-OXAZOLIDINE-4-(2',2'-DIFLUORO-3'-HYDROXY)-PROPANOATE
SpectraBase Compound ID E3VXVyKla2K
InChI InChI=1S/C27H23F2NO5/c1-2-34-24(32)27(28,29)23(31)22-16-35-25(33)30(22)26(17-10-4-3-5-11-17)20-14-8-6-12-18(20)19-13-7-9-15-21(19)26/h3-15,22-23,31H,2,16H2,1H3/t22-,23-/m0/s1
InChIKey KYUNZYGSPZTZQM-GOTSBHOMSA-N
Mol Weight 479.48 g/mol
Molecular Formula C27H23F2NO5
Exact Mass 479.154429 g/mol
Enantiomer InChIKey KYUNZYGSPZTZQM-DHIUTWEWSA-N

View Spectrum of ETHYL-(4S,3'S)-2-OXO-3-(9-PHENYLFLUOREN-9-YL)-OXAZOLIDINE-4-(2',2'-DIFLUORO-3'-HYDROXY)-PROPANOATE

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

View Spectrum of ETHYL-(4S,3'S)-2-OXO-3-(9-PHENYLFLUOREN-9-YL)-OXAZOLIDINE-4-(2',2'-DIFLUORO-3'-HYDROXY)-PROPANOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
ETHYL-(4S,3'R)-2-OXO-3-(9-PHENYLFLUOREN-9-YL)-OXAZOLIDINE-(2',2'-DIFLUORO-3'-HYDROXY)-PROPANOATE
(4S,5S)-4-METHYL-5-[[(1'S)-PHENYLETHYL]-CARBAMOYL]-1-(9''-PHENYLFLUOREN-9''-YL)-2-PYRROLIDONE
(13R*,13aS*)-7,8,13,13a-Tetrahydro-10,11-dimethoxy-13-phenyl-5H-isoindolo[1,2-b][3]benzazepin-5-one
METHYL-N-[4-OXO-4-[(3-BETA,22E)-STIGMASTA-5,22-DIEN-3-YLOXY]-BUTANOYL]-L-PHENYLALANINE
No Name
XBQHZZWIVHCCBK-UHFFFAOYSA-N
Coumachlor-A (-H2O)
2-(1',2'-DIHYDROXYPROPYL)-4-(2''-ETHYLPROP-2''-ENYLOXY)-1-METHOXYANTHRAQUINONE
4-(2-Amino-3-cyano-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromen-4-yl)-3,5-dimethyl-1H-pyrrole-2-carbonitrile
4-BENZOYL-1-BENZYL-5-PARA-DIMETHYLAMINOPHENYL-2,3,4,5-TETRAHYDRO-1-H-PYRROLE-2,3-DIONE
Title Journal or Book Year
Synthesis of l-4,4-Difluoroglutamic Acid via Nucleophilic Addition to a Chiral Aldehyde The Journal of Organic Chemistry 2001

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