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#22B;1-[N-BENZYLOXYCARBONYL-(1S,2S)-1-AMINO-3,3-DIFLUORO-3-ETHOXYCARBONYL-4-OXYTHIOCARBONYLIMIDAZOLEPROPYL]-4-METHYL-2,6,7-TRIOXABICYCLO-[2.2.2]-OCTANE

Compound with spectra: 1 NMR

#22B;1-[N-BENZYLOXYCARBONYL-(1S,2S)-1-AMINO-3,3-DIFLUORO-3-ETHOXYCARBONYL-4-OXYTHIOCARBONYLIMIDAZOLEPROPYL]-4-METHYL-2,6,7-TRIOXABICYCLO-[2.2.2]-OCTANE
SpectraBase Compound ID F6qM6zKLu7b
InChI InChI=1S/C24H27F2N3O8S/c1-3-32-19(30)23(25,26)18(37-21(38)29-10-9-27-15-29)17(24-34-12-22(2,13-35-24)14-36-24)28-20(31)33-11-16-7-5-4-6-8-16/h4-10,15,17-18H,3,11-14H2,1-2H3,(H,28,31)/t17-,18+,22?,24?/m0/s1
InChIKey XJWAKEKEVOTDTM-ZOOZGXBGSA-N
Mol Weight 555.55 g/mol
Molecular Formula C24H27F2N3O8S
Exact Mass 555.148692 g/mol
Enantiomer InChIKey XJWAKEKEVOTDTM-NGHOGTAGSA-N

View Spectrum of #22B;1-[N-BENZYLOXYCARBONYL-(1S,2S)-1-AMINO-3,3-DIFLUORO-3-ETHOXYCARBONYL-4-OXYTHIOCARBONYLIMIDAZOLEPROPYL]-4-METHYL-2,6,7-TRIOXABICYCLO-[2.2.2]-OCTANE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#22A+22B;1-[N-BENZYLOXYCARBONYL-(1S,2R/S)-1-AMINO-3,3-DIFLUORO-3-ETHOXYCARBONYL-4-OXYTHIOCARBONYLIMIDAZOLEPROPYL]-4-METHYL-2,6,7-TRIOXABICYCLO-[2.2.2]-OCTANE
#22A;1-[N-BENZYLOXYCARBONYL-(1S,2R)-1-AMINO-3,3-DIFLUORO-3-ETHOXYCARBONYL-4-OXYTHIOCARBONYLIMIDAZOLEPROPYL]-4-METHYL-2,6,7-TRIOXABICYCLO-[2.2.2]-OCTANE
ETHYL-2,2-BIS-[5-(4-METHYLPHENYL)-2-PHENYL-1,2,4-TRIAZOL-3-YL]-ACETATE
(+/-)-1beta-(Benzyloxycarbonylamino)-2alpha,3alpha-dihydroxy-2alpha,3alpha-O-isopropylidene-4-methylidene-cyclopentane oxide
benzenesulfonamide, N-[[5-(2-aminophenyl)-1-(2-methylpropyl)-1H-imidazol-4-yl]carbonyl]-4-methyl-
.beta.-L-Allofuranuronic acid, 2,3-O-(1-methylethylidene)-, methyl ester, 5-(3-chlorobenzoate)
ETHYL-2,2-BIS-(2,5-DIPHENYL-1,2,4-TRIAZOL-3-YL)-ACETATE
2-(4-(Benzyloxy)phenyl)-1,4,5-triphenyl-1H-imidazole
3-(3-bromophenyl)-5-[2-nitro-5-(trifluoromethyl)phenyl]sulfanyl-4-phenyl-1,2,4-triazole
1-(2,4-difluorophenyl)-3-(4-methylphenyl)-5-(2-thienyl)-4,5-dihydro-1H-pyrazole
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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