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(2S,3S,3aS,5S)-1,2,3,3a,4,5-Hexahydropyrrolo[1,2-a]quinoline-2,3,5-triol

Compound with spectra: 2 NMR, and 1 MS (GC)

(2S,3S,3aS,5S)-1,2,3,3a,4,5-Hexahydropyrrolo[1,2-a]quinoline-2,3,5-triol
SpectraBase Compound ID ErOt6lYVUtA
InChI InChI=1S/C12H15NO3/c14-10-5-9-12(16)11(15)6-13(9)8-4-2-1-3-7(8)10/h1-4,9-12,14-16H,5-6H2/t9-,10-,11-,12-/m0/s1
InChIKey CPXBNVXRILVTKQ-BJDJZHNGSA-N
Mol Weight 221.26 g/mol
Molecular Formula C12H15NO3
Exact Mass 221.105193 g/mol
Enantiomer InChIKey CPXBNVXRILVTKQ-DDHJBXDOSA-N

View Spectrum of (2S,3S,3aS,5S)-1,2,3,3a,4,5-Hexahydropyrrolo[1,2-a]quinoline-2,3,5-triol

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum U1-2014-7129-27a

View Spectrum of (2S,3S,3aS,5S)-1,2,3,3a,4,5-Hexahydropyrrolo[1,2-a]quinoline-2,3,5-triol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of (2S,3S,3aS,5S)-1,2,3,3a,4,5-Hexahydropyrrolo[1,2-a]quinoline-2,3,5-triol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
(3S,3AR,5R)-3-(TERT.-BUTOXY)-1,2,3,3A,4,5-HEXAHYDRO-PYRROLO-[1,2-A]-QUINOLIN-5-OL
(3S,3AS,5S)-3-(TERT.-BUTOXY)-1,2,3,3A,4,5-HEXAHYDRO-PYRROLO-[1,2-A]-QUINOLIN-5-OL
1-ACETYL-3,4-EPOXY-2-METHYL-1,2,3,4-TETRAHYDROQUINOLINE
(4aR,9aS)-2-(t-Butyl)-10-[2'-(1'-piperidyl)ethyl]-(octahydro)-acridine-maleate
3,3-BIS-(3-METHYLBUTYL)-4-HYDROXY-N-METHYL-2,4-QUINOLONE
(4aS,9aS)-2-(t-Butyl)-10-[2'-(1'-pyrrolidinyl)ethyl]-(octahydro)-acridine-maleate
1-[2-(4-chloro-2-methylphenoxy)propanoyl]-6-fluoro-2-methyl-1,2,3,4-tetrahydroquinoline
(4aR,9aR)-2-(t-Butyl)-10-[2'-(diethylamino)ethyl]-(octahydro)-acridine-maleate
(4aR,9aS)-2-(t-Butyl)-10-[2'-(diethylamino)ethyl]-(octahydro)-acridine-maleate
Benzyl 4,5-Dimethoxytetrahydrobenzazepine-1-carboxylate
Title Journal or Book Year
Modular Access to Highly Functionalised Tetrahydroquinolines European Journal of Organic Chemistry 2014
Copper-Catalyzed Synthesis of a Highly Hydroxy-Functionalized Benzo[e]indolizidine by IntramolecularN-Arylation European Journal of Organic Chemistry 2013
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