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#-20;METHYL-(9R*,9AS*,10R*)-10-ALLYL-9-[[TERT.-BUTYL-(DIMETHYL)-SILOXY]-ETHYL]-9-HYDROXY-6-OXO-6,7,8,9,9A,10-HEXAHYDROPYRIDO-[1,2-A]-INDOL-10-CARBOXYLATE

Compound with spectra: 1 NMR

#-20;METHYL-(9R*,9AS*,10R*)-10-ALLYL-9-[[TERT.-BUTYL-(DIMETHYL)-SILOXY]-ETHYL]-9-HYDROXY-6-OXO-6,7,8,9,9A,10-HEXAHYDROPYRIDO-[1,2-A]-INDOL-10-CARBOXYLATE
SpectraBase Compound ID JEOOFDRaNhz
InChI InChI=1S/C25H37NO5Si/c1-8-14-25(22(28)30-5)18-11-9-10-12-19(18)26-20(27)13-15-24(29,21(25)26)16-17-31-32(6,7)23(2,3)4/h8-12,21,29H,1,13-17H2,2-7H3/t21-,24+,25-/m0/s1
InChIKey IVLDLVQVOCXLCT-GPUOULLFSA-N
Mol Weight 459.7 g/mol
Molecular Formula C25H37NO5Si
Exact Mass 459.2441 g/mol
Enantiomer InChIKey IVLDLVQVOCXLCT-IEZKXTBUSA-N

View Spectrum of #-20;METHYL-(9R*,9AS*,10R*)-10-ALLYL-9-[[TERT.-BUTYL-(DIMETHYL)-SILOXY]-ETHYL]-9-HYDROXY-6-OXO-6,7,8,9,9A,10-HEXAHYDROPYRIDO-[1,2-A]-INDOL-10-CARBOXYLATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
Novel Stereoselective Syntheses of Highly Functionalized Benzannulated Pyrrolizidines and Indolizidines by Samarium Diiodide Induced Cyclizations of Indole Derivatives Organic Letters 2003
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