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METHYL-(1RS,5SR,6SR)-2-(2-HYDROXYETHYL)-6-(METHOXYCARBONYL)-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-4-(E)-ACRYLATE

Compound with spectra: 1 NMR

METHYL-(1RS,5SR,6SR)-2-(2-HYDROXYETHYL)-6-(METHOXYCARBONYL)-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-4-(E)-ACRYLATE
SpectraBase Compound ID BpYwegjBwCz
InChI InChI=1S/C22H24N2O5/c1-28-18(26)8-7-13-12-24(9-10-25)17-11-15(13)20(22(27)29-2)19-14-5-3-4-6-16(14)23-21(17)19/h3-8,12,15,17,20,23,25H,9-11H2,1-2H3/b8-7+/t15?,17?,20-/m0/s1
InChIKey YWAOLDFDDQABKT-HSGJSHHASA-N
Mol Weight 396.44 g/mol
Molecular Formula C22H24N2O5
Exact Mass 396.168522 g/mol
Enantiomer InChIKey YWAOLDFDDQABKT-FESCVBIWSA-N

View Spectrum of METHYL-(1RS,5SR,6SR)-2-(2-HYDROXYETHYL)-6-(METHOXYCARBONYL)-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-4-(E)-ACRYLATE

13C NMR Spectrum
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Solvent DMSO-D6
METHYL-(1RS,5RS,6RS)-2-(2-HYDROXYETHYL)-6-(METHOXYCARBONYL)-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-4-(E)-ACRYLATE
Title Journal or Book Year
General method for the synthesis of bridged indole alkaloids. Nucleophilic addition of indoleacetic ester enolates to N-alkylpyridinium salts The Journal of Organic Chemistry 1990
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Unknown Identification

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