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METHYL_3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE

Compound with spectra: 1 NMR

METHYL_3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE
SpectraBase Compound ID 6tWC5xR5rp6
InChI InChI=1S/C19H24N2O3/c1-11(22)12-9-15(19(23)24-2)18-17-14(7-8-21(18)10-12)13-5-3-4-6-16(13)20-17/h3-6,11-12,15,18,20,22H,7-10H2,1-2H3/t11-,12-,15-,18-/m1/s1
InChIKey DLZVQMJHFNDYKK-CBBSBYJHSA-N
Mol Weight 328.41 g/mol
Molecular Formula C19H24N2O3
Exact Mass 328.178693 g/mol
Enantiomer InChIKey DLZVQMJHFNDYKK-LLXPTAGJSA-N

View Spectrum of METHYL_3-ALPHA-(1'-ALPHA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-CARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Methyl (1S,3S,12bS)-3-(1-hydroxyethyl)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-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'-BETA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-BETA-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_3-ALPHA-(1'-BETA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE
(1S,3R,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine-1-carboxylic acid methyl ester
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
(1S,3E,12bR)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine-1-carboxylic acid methyl ester
E-trans-Methyl 3-Ethylideneoctahydropyridino[1,2-a]carbolinecarboxylate
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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