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(2S)-2-[(1R)-1-[(1R)-2-OXO-1-PHENOXY-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-PHENOXY-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER
SpectraBase Compound ID AuQGqRv0TKV
InChI InChI=1S/C24H34N2O4/c1-5-19(20-14-11-17-26(20)23(28)30-24(2,3)4)21(22(27)25-15-9-10-16-25)29-18-12-7-6-8-13-18/h5-8,12-13,19-21H,1,9-11,14-17H2,2-4H3/t19-,20+,21-/m1/s1
InChIKey VDKLCTBDCFCOMR-QHAWAJNXSA-N
Mol Weight 414.5 g/mol
Molecular Formula C24H34N2O4
Exact Mass 414.251858 g/mol
Enantiomer InChIKey VDKLCTBDCFCOMR-HBMCJLEFSA-N

View Spectrum of (2S)-2-[(1R)-1-[(1R)-2-OXO-1-PHENOXY-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-(4-FLUOROPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER
(1R,2R,7AS)-1-ETHENYL-2-(2-BROMO-3-METHYLPHENOXY)-PYRROLIZIDIN-3-ONE
(1R,2S,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
(4aS*,8aS*)-4-(Benzyloxycarbonyl)-8a-ethenyl-2-oxo-3,4,4a,5,6,7,8,8a-octahydro-2H-1,4-benzoxazine
TERT.-BUTYL-(2S)-2-[(1R)-1-ACRYLOYLOXY-1-[2-(1,3-DIOXOLAN-2-YL)-ETHYL]-2-PROPENYL]-TETRAHYDROPYRROLE-1-CARBOXYLATE;(2S,1'R)-ISOMER
RAC-2,2,5,5-TETRAMETHYL-7-PHENOXY-3-OXA-1-AZABICYCLO-[4.2.0]-OCTAN-8-ONE
(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
N-Formylnorcocain
2RS(2R*,3R*,3aS*)-2,3,3a,4,5,6-hexahydro-3-phenyl-2-piperidinocarbonylpyrrolo[1,2-b]isoxazole
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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