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(2S)-2-[(1R)-1-[(1R)-2-OXO-1-(3-CHLOROPHENOXY)-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-(3-CHLOROPHENOXY)-2-(1-PYROLIDINYL)-ETHYL]-2-PROPEN-1-YL]-1-PYRROLIDINE-CARBOXYLIC-ACID-TERT.-BUTYLESTER
SpectraBase Compound ID Dzul7YvEMiF
InChI InChI=1S/C24H33ClN2O4/c1-5-19(20-12-9-15-27(20)23(29)31-24(2,3)4)21(22(28)26-13-6-7-14-26)30-18-11-8-10-17(25)16-18/h5,8,10-11,16,19-21H,1,6-7,9,12-15H2,2-4H3/t19-,20+,21-/m1/s1
InChIKey RRYOQMSNIPIJIJ-QHAWAJNXSA-N
Mol Weight 449.0 g/mol
Molecular Formula C24H33ClN2O4
Exact Mass 448.212885 g/mol
Enantiomer InChIKey RRYOQMSNIPIJIJ-HBMCJLEFSA-N

View Spectrum of (2S)-2-[(1R)-1-[(1R)-2-OXO-1-(3-CHLOROPHENOXY)-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-[2R*[(R*),.alpha.(R*),.beta.(S*)]]]-1-[1,1-Dimethylethoxycarbonyl]-.beta.-hydroxy-.alpha.-methyl-2-pyrrolidinepropanoic Acid 2-Hydroxy-1,2,2-triphenylethyl Ester
5H-4-Oxa-5a-azabenz[cd]azulen-5-one, 1,2,6,7,8,9,9a,9b-octahydro-3-phenyl-, trans-
2,3-CYCLOPROPANE-3-TRIMETHYLSILYLOXY-8-AZA-BICYCLO-[3.2.1]-OCTANE-8-CARBOXYLIC-ACID-ETHYLESTER
N-TERT.-BUTYLOXYCARBONYL-2-METHYLAMINO-PROPIONIC-ACID-[3-(1,3-DIHYDRO-1,3-DIOXO-2H-ISOINDOLE-2-YL)-2,6-DIOXO-PIPERIDINE-1-YL-METHYL]-ESTER
#17H;(2R,3R)-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,4R)-4-METHOXY-2-(METHOXYMETHYL)-PYRROLIDIN-1-YL]-2-[2-(3-METHOXYPHENYL)-ETHYL]-4-METHYLPENT-4-EN-1-
PERFLUOROMETHYL(2,4-DIMETHYL-1,3-DIOXOLAN-2-YL)KETONE, N-METHYL-N-PHENYLHYDRAZONE (ISOMER MIXTURE)
(4aR,8aR)-7-keto-4a-(pyrrolidine-1-carbonyl)-3,4,8,8a-tetrahydro-1H-isoquinoline-2-carboxylic acid ethyl ester
tert-Butyl (2-((5S,6S)-5-((tert-butyldimethylsilyl)oxy)-6-(2-(methoxy-methoxy)-5-vinylphenoxy)cyclohex-1-en-1-yl)ethyl)(methyl)carbamate
(CIS)-(3AS,4S,9AS,9BR)-4-ETHYL-2,2-DIMETHYLHEXAHYDRO-[1,3]-DIOXOLO-[4,5-G]-INDOLIZIN-7(3AH)-ONE
(7'-S,8'-S)-NOCOMTAL
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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