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(2S)-2-[(1R)-1-[(1R)-2-OXO-1-(4-FLUOROPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER

Compound with spectra: 1 NMR

(2S)-2-[(1R)-1-[(1R)-2-OXO-1-(4-FLUOROPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER
SpectraBase Compound ID 5p9OMZpwu78
InChI InChI=1S/C24H33FN2O4/c1-5-19(20-9-8-16-27(20)23(29)31-24(2,3)4)21(22(28)26-14-6-7-15-26)30-18-12-10-17(25)11-13-18/h5,10-13,19-21H,1,6-9,14-16H2,2-4H3/t19-,20+,21-/m1/s1
InChIKey ZDWCXXIDGUJQNP-QHAWAJNXSA-N
Mol Weight 432.5 g/mol
Molecular Formula C24H33FN2O4
Exact Mass 432.242436 g/mol
Enantiomer InChIKey ZDWCXXIDGUJQNP-HBMCJLEFSA-N

View Spectrum of (2S)-2-[(1R)-1-[(1R)-2-OXO-1-(4-FLUOROPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S)-2-[(1R)-1-[(1R)-2-OXO-1-PHENOXY-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER
(1R,2S,7AS)-1-ETHENYL-2-(2-BROMO-3-METHYLPHENOXY)-PYRROLIZIDIN-3-ONE
(1R,2R,7AS)-1-ETHENYL-2-(2-BROMO-3-METHYLPHENOXY)-PYRROLIZIDIN-3-ONE
(4aR,8aR)-Ethyl 4a-methoxy-7-oxo-3,4,4a,7,8,8a-hexahydro-2H-quinoline-1-carboxylate
2-Azetidinone, 3-(4-chlorophenoxy)-1-[(4-fluorophenyl)methyl]-4-(3,4,5-trimethoxyphenyl)-
(2R,4S,5R,6R)-6-[(R)-2-Hydroxybut-3-enyl]-4,5-dihydroxy-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester
TERT.-BUTYL-(2S)-2-[(1S)-1-ACRYLOYLOXY-1-[2-(1,3-DIOXOLAN-2-YL)-ETHYL]-2-PROPENYL]-TETRAHYDROPYRROLE-1-CARBOXYLATE;(2S,1'S)-ISOMER
TERT.-BUTYL-(2S)-2-[(1R)-1-ACRYLOYLOXY-1-[2-(1,3-DIOXOLAN-2-YL)-ETHYL]-2-PROPENYL]-TETRAHYDROPYRROLE-1-CARBOXYLATE;(2S,1'R)-ISOMER
(2S,3aR,6S,7aR)-6-hydroxy-2,3,3a,6,7,7a-hexahydroindole-1,2-dicarboxylic acid O1-benzyl ester O2-methyl ester
(4aS*,8aS*)-4-(Benzyloxycarbonyl)-8a-ethenyl-2-oxo-3,4,4a,5,6,7,8,8a-octahydro-2H-1,4-benzoxazine
Title Journal or Book Year
1,2-Asymmetric Induction in Diastereo­selective Zwitterionic Aza-Claisen Rearrangements: Key Steps in Optically Active Alkaloid Synthesis European Journal of Organic Chemistry 2013
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