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#-(4R)-5-(S)-MOSHERESTER;(4R,1'S,2''S)-4-[1'-TERT.-BUTOXYCARBONYLAMINO-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLOXY)-ETHYL]-6-METHYL-2-OXO-1,

Compound with spectra: 1 NMR

#-(4R)-5-(S)-MOSHERESTER;(4R,1'S,2''S)-4-[1'-TERT.-BUTOXYCARBONYLAMINO-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLOXY)-ETHYL]-6-METHYL-2-OXO-1,
SpectraBase Compound ID 4TmH3PbdO7q
InChI InChI=1S/C25H32F3N3O8/c1-7-37-19(32)17-14(2)29-21(34)31-18(17)16(30-22(35)39-23(3,4)5)13-38-20(33)24(36-6,25(26,27)28)15-11-9-8-10-12-15/h8-12,16,18H,7,13H2,1-6H3,(H,30,35)(H2,29,31,34)/t16-,18+,24-/m0/s1
InChIKey XSTZVAUTXFNWCR-GXYVPTEVSA-N
Mol Weight 559.5 g/mol
Molecular Formula C25H32F3N3O8
Exact Mass 559.214149 g/mol
Enantiomer InChIKey XSTZVAUTXFNWCR-SDWUMEBZSA-N

View Spectrum of #-(4R)-5-(S)-MOSHERESTER;(4R,1'S,2''S)-4-[1'-TERT.-BUTOXYCARBONYLAMINO-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLOXY)-ETHYL]-6-METHYL-2-OXO-1,

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
#-(4R)-5-(R)-MOSHERESTER;(4R,1'S,2''R)-4-[1'-TERT.-BUTOXYCARBONYLAMINO-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLOXY)-ETHYL]-6-METHYL-2-OXO-1,
#-20-(R)-MOSHERESTER;MINOR-DIASTEREOMER;(1'R,2''R)-4-[1'-TERT.-BUTOXYCARBONYLAMINO-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLOXY)-ETHYL]-2,6-D
#-20-(R)-MOSHERESTER;MAJOR-DIASTEREOMER;(1'S,2''R)-4-[1'-TERT.-BUTOXYCARBONYLAMINO-2'-(3'',3'',3''-TRIFLUORO-2''-METHOXY-2''-PHENYL-PROPIONYLOXY)-ETHYL]-2,6-D
(6S,7S)-cis-6,7-dihydroxy-4,5,6,7-tetrahydrobenzofuran bis(MTPA) dev.
ethyl 4-[5-(2-chloro-4-nitrophenyl)-2-furyl]-6-methyl-2-oxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate
(1R)-1-[(5R)-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}-4-methyl-2-oxo-2,5-dihydrofuran-3-yl]-2-methylpropyl (2R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
(1R)-1-[(5R)-5-{[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxy}-4-methyl-2-oxo-2,5-dihydrofuran-3-yl]-2-methylpropyl (2S)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
5-Pyrimidinecarboxylic acid, 4-(2,5-dimethylphenyl)-1,2,3,4-tetrahydro-6-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-2-oxo-, ethyl ester
5-pyrimidinecarboxylic acid, 6-[[(4-fluorophenyl)sulfonyl]methyl]-1,2,3,4-tetrahydro-4-(4-hydroxy-3-methoxyphenyl)-2-oxo-, ethyl ester
2-phenoxyethyl 1,6-dimethyl-4-(2-nitrophenyl)-2-oxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate
Title Journal or Book Year
Model Studies toward the Synthesis of Dihydropyrimidinyl and Pyridyl α-Amino Acids via Three-Component Biginelli and Hantzsch Cyclocondensations The Journal of Organic Chemistry 2003
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