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(2R*,5S*,11R*)Methyl 4,6-Dimethyl-1-oxo-3,4-oxaza-1,2,3,4,5,6-hexahydro-2,5-methanocyclohepta[b]indole-11-carboxylate

Compound with spectra: 1 NMR, and 1 MS (GC)

(2R*,5S*,11R*)Methyl 4,6-Dimethyl-1-oxo-3,4-oxaza-1,2,3,4,5,6-hexahydro-2,5-methanocyclohepta[b]indole-11-carboxylate
SpectraBase Compound ID aHYca0adXK
InChI InChI=1S/C16H16N2O4/c1-17-9-7-5-4-6-8(9)10-12(17)13-11(16(20)21-3)15(14(10)19)22-18(13)2/h4-7,11,13,15H,1-3H3/t11-,13+,15-/m1/s1
InChIKey OZJPUJSNSDTBAQ-OSAQELSMSA-N
Mol Weight 300.31 g/mol
Molecular Formula C16H16N2O4
Exact Mass 300.111007 g/mol
Enantiomer InChIKey OZJPUJSNSDTBAQ-LNSITVRQSA-N

View Spectrum of (2R*,5S*,11R*)Methyl 4,6-Dimethyl-1-oxo-3,4-oxaza-1,2,3,4,5,6-hexahydro-2,5-methanocyclohepta[b]indole-11-carboxylate

MS (GC) Spectrum
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Source of Spectrum KC-0-955-11

View Spectrum of (2R*,5S*,11R*)Methyl 4,6-Dimethyl-1-oxo-3,4-oxaza-1,2,3,4,5,6-hexahydro-2,5-methanocyclohepta[b]indole-11-carboxylate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2R*,5S*,11S*)Methyl 4,6-Dimethyl-1-oxo-3,4-oxaza-1,2,3,4,5,6-hexahydro-2,5-methanocyclohepta[b]indole-11-carboxylate
Title Journal or Book Year
Synthesis of indole substituted dihydro- and tetrahydro-isoxazoles via 1,3-dipolar cycloadditions of C-(1-methylindol-2-yl)-N -methylnitrone with unsaturated carbonyl derivatives and a study of their acid-induced intramolecular cyclizations Journal of the Chemical Society, Perkin Transactions 1 1997
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