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METHYL-(1RS,5SR,6SR)-4-(E)-ETHYLIDENE-2-METHYL-1,2,3,4,5,6-HEXAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-6-CARBOXYLATE

Compound with spectra: 1 NMR

METHYL-(1RS,5SR,6SR)-4-(E)-ETHYLIDENE-2-METHYL-1,2,3,4,5,6-HEXAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-6-CARBOXYLATE
SpectraBase Compound ID 59ArsMRYz9g
InChI InChI=1S/C19H22N2O2/c1-4-11-10-21(2)15-9-13(11)17(19(22)23-3)16-12-7-5-6-8-14(12)20-18(15)16/h4-8,13,15,17,20H,9-10H2,1-3H3/b11-4+/t13?,15?,17-/m0/s1
InChIKey OPJLIXGOQRYGFW-CNWHHZNCSA-N
Mol Weight 310.4 g/mol
Molecular Formula C19H22N2O2
Exact Mass 310.168128 g/mol
Enantiomer InChIKey OPJLIXGOQRYGFW-ZULFJXGGSA-N

View Spectrum of METHYL-(1RS,5SR,6SR)-4-(E)-ETHYLIDENE-2-METHYL-1,2,3,4,5,6-HEXAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-6-CARBOXYLATE

13C NMR Spectrum
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Solvent CDCl3
METHYL-(1RS,5SR,6RS)-4-(E)-ETHYLIDENE-2-METHYL-1,2,3,4,5,6-HEXAHYDRO-1,5-METHANOAZOCINO-[3,4-B]-INDOLE-6-CARBOXYLATE
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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