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

Compound with spectra: 1 NMR

(1RS,5RS,6SR)-2-(2-ACETOXYETHYL)-6-(METHOXYCARBONYL)-7-METHYL-1,2,5,6-TETRAHYDRO-1,5-METHANOAZOCINO-[4,3-B]-INDOLE-4-(E)-ACRYLATE
SpectraBase Compound ID 1OwzDNRgsVw
InChI InChI=1S/C25H28N2O6/c1-15(28)33-12-11-27-14-16(9-10-21(29)31-3)18-13-20(27)22-17-7-5-6-8-19(17)26(2)24(22)23(18)25(30)32-4/h5-10,14,18,20,23H,11-13H2,1-4H3/b10-9+/t18?,20?,23-/m1/s1
InChIKey VAWFMAFBDJBWJZ-YNGXNVNWSA-N
Mol Weight 452.51 g/mol
Molecular Formula C25H28N2O6
Exact Mass 452.194737 g/mol
Enantiomer InChIKey VAWFMAFBDJBWJZ-RGNNYTDDSA-N

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

13C NMR Spectrum
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Solvent CDCl3
METHYL-(1RS,5SR,6RS)-2-(2-ACETOXYETHYL)-6-(METHOXYCARBONYL)-7-METHYL-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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