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(1S,12bS)-10-nitro-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

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

(1S,12bS)-10-nitro-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester
SpectraBase Compound ID ByBI0VzeCFP
InChI InChI=1S/C17H19N3O4/c1-24-17(21)13-3-2-7-19-8-6-12-11-5-4-10(20(22)23)9-14(11)18-15(12)16(13)19/h4-5,9,13,16,18H,2-3,6-8H2,1H3/t13-,16-/m0/s1
InChIKey PYMCRCAEFFWWHT-BBRMVZONSA-N
Mol Weight 329.36 g/mol
Molecular Formula C17H19N3O4
Exact Mass 329.137556 g/mol
Enantiomer InChIKey PYMCRCAEFFWWHT-CZUORRHYSA-N

View Spectrum of (1S,12bS)-10-nitro-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum H1-50-247-4

View Spectrum of (1S,12bS)-10-nitro-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1S,12bS)-10-nitro-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]$b-carboline-1-carboxylic acid methyl ester

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
  • Methyl 10-Nitroindolo[2,3-a]quinolizidine-1-carboxylate
TRANS-EPIMER
CIS-EPIMER
METHYL-10-METHOXY-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2,3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE;CIS-ESTER
METHYL-10-METHOXY-1,2,3,4,6,7,12,12B-ALPHA-OCTAHYDROINDOLO-[2,3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE;TRANS-ESTER
(1S,3S,12bR)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-carboxylic acid methyl ester
1-BETA-METHOXYCARBONYL-3-BETA-ETHYLINDOLO-[2,3-A]-QUINOLIZIDINE
1-ALPHA-METHOXYCARBONYL-3-BETA-ETHYLINDOLO-[2,3-A]-QUINOLIZIDINE
Methyl 3-.alpha.-ethyl-1,2,3,4,6,7,12,12b.beta.-octahydroindolo[2,3-a]quinolizine-1.alpha.-carboxylate
METHYL-3-ALPHA-ETHYL-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2,3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE
1-ALPHA-METHOXYCARBONYL-3-ALPHA-ETHYLINDOLO-[2,3-A]-QUINOLIZIDINE
Title Journal or Book Year
Substituent Effects on the Rate of Acid-catalysed Epimerization of Indolo[2,3-a]quinolizidines HETEROCYCLES 1999
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