For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

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

Compound with spectra: 1 NMR

METHYL_3-ALPHA-(1'-BETA-HYDROXYETHYL)-1,2,3,4,6,7,12,12B-BETA-OCTAHYDROINDOLO-[2.3-A]-QUINOLIZINE-1-ALPHA-CARBOXYLATE
SpectraBase Compound ID 1289Jy3bEjo
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+/m0/s1
InChIKey DLZVQMJHFNDYKK-ZQUVKOLYSA-N
Mol Weight 328.41 g/mol
Molecular Formula C19H24N2O3
Exact Mass 328.178693 g/mol
Enantiomer InChIKey DLZVQMJHFNDYKK-IPTNHLRFSA-N

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

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.