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3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLIC_ACID_LACTONE

Compound with spectra: 1 NMR

3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLIC_ACID_LACTONE
SpectraBase Compound ID DyyHlbPmXUg
InChI InChI=1S/C18H20N2O2/c1-10-11-8-14(18(21)22-10)17-16-13(6-7-20(17)9-11)12-4-2-3-5-15(12)19-16/h2-5,10-11,14,17,19H,6-9H2,1H3/t10-,11-,14+,17-/m1/s1
InChIKey DRHFEZKLNCBOOT-DNAIWCKFSA-N
Mol Weight 296.37 g/mol
Molecular Formula C18H20N2O2
Exact Mass 296.152478 g/mol
Enantiomer InChIKey DRHFEZKLNCBOOT-ROKSBRBMSA-N

View Spectrum of 3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLIC_ACID_LACTONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
3-ALPHA-(1'-BETA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-CARBOXYLIC_ACID_LACTONE
(1S,3R,12bR)-3-[(1R)-1-trimethylsilyloxyethyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-carboxylic acid methyl ester
METHYL_3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE
Methyl 3-(1.alpha.-hydroxyethyl)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1.alpha.-carboxylate
METHYL_3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE
Methyl (1S,3S,12bS)-3-(1-hydroxyethyl)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-carboxylate
METHYL_3-ALPHA-(1'-BETA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE
METHYL_3-ALPHA-(1'-BETA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE
3-Acetyl-1-(methoxycarbonyl)indolo[2,3-a]quinolizine
(1R,5R,14bS)-4-methyl-3,4,5,6,8,9,14,14b-octahydro-1,5-methanoazocino[1',2':1,2]pyrido[3,4-b]indol-2(1H)-one
Title Journal or Book Year
Lactone Formation as an Aid in the NMR Characterization of Two 3-(1'-Hydroxyethyl)indolo[2,3-a]qunolizidine-1-carboxylates: Intermediates for the Stereoselective Synthesis of Tacamine-Type Indole Alkaloids HETEROCYCLES 1997
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