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METHYL-(1RS,5SR,6RS)-6-(METHOXYCARBONYL)-2,7-DIMETHYL-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[4,3-B]-INDOLE-4-(E)-ACRYLATE

Compound with spectra: 1 NMR

METHYL-(1RS,5SR,6RS)-6-(METHOXYCARBONYL)-2,7-DIMETHYL-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[4,3-B]-INDOLE-4-(E)-ACRYLATE
SpectraBase Compound ID 9yuq3IKrTVJ
InChI InChI=1S/C22H24N2O4/c1-23-12-13(9-10-18(25)27-3)15-11-17(23)19-14-7-5-6-8-16(14)24(2)21(19)20(15)22(26)28-4/h5-10,12,15,17,20H,11H2,1-4H3/b10-9+/t15?,17?,20-/m0/s1
InChIKey HETKLIGLCQMFAM-WIMHSHKZSA-N
Mol Weight 380.44 g/mol
Molecular Formula C22H24N2O4
Exact Mass 380.173607 g/mol
Enantiomer InChIKey HETKLIGLCQMFAM-QLGYKBHESA-N

View Spectrum of METHYL-(1RS,5SR,6RS)-6-(METHOXYCARBONYL)-2,7-DIMETHYL-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[4,3-B]-INDOLE-4-(E)-ACRYLATE

13C NMR Spectrum
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Solvent CDCl3
(1RS,5SR,6SR)-6-(METHOXYCARBONYL)-2,7-DIMETHYL-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[4,3-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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