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

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

(2R*,5S*)-4,6-Dimethyl-1-oxo-3,4-oxaza-1,2,3,4,5,6-hexahydro-2,5-methanocyclohepta[b]indole
SpectraBase Compound ID L06Xt380bzl
InChI InChI=1S/C14H14N2O2/c1-15-9-6-4-3-5-8(9)12-13(15)10-7-11(14(12)17)18-16(10)2/h3-6,10-11H,7H2,1-2H3/t10-,11+/m0/s1
InChIKey UCONNPKNKDETIT-WDEREUQCSA-N
Mol Weight 242.28 g/mol
Molecular Formula C14H14N2O2
Exact Mass 242.105528 g/mol
Enantiomer InChIKey UCONNPKNKDETIT-MNOVXSKESA-N

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

MS (GC) Spectrum
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Source of Spectrum KC-0-956-11

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

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1,1-Dimethylethyl 1-(2-(4-methylphenyl)-1H-indol-3-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
6-(p-CHLOROBENZOYL)-2,9-DIBROMO-7H-BENZO[c]FLUORENE-7-ONE
4,5,6,7-tetrachloro-2-methyl-3-[N'-(4''-methylphenyl)succinimido]isoindolin-1-one
(E)-3-(3-Cyclopropyl-1-(4-bromobenzylidene)-1H-inden-2-yl)-1-methyl-1H-indole
(Z)-3-(3-Cyclopropyl-1-(4-bromobenzylidene)-1H-inden-2-yl)-1-methyl-1H-indole
(E)-2-(2,4,5-Trifluoro-3-(2-methoxy-4-(prop-1-enyl)phenoxy)-6-(pyridin-2-yl)phenyl)benzoxazole
1,2-bis(propylsulfonyl)-7-(4-pyridinyl)-3-indolizinecarboxamide
(R)-9-BENZYL-2-[(R)-2-HYDROXY-1-PHENYLETHYL]-1-PROPYL-1,2,3,4-TETRAHYDROPYRIDO-[3,4-B]-INDOLE
(S)-9-Benzyl-2-[(R)-2-hydroxy-1-phenylethyl]-1-propyl-1,2,3,4-tetrahydropyrido[3,4-b]indole
1H-Pyrido[3,4-b]indole-3-carboxamide, 2,3,4,9-tetrahydro-2-hydroxy-N,9-dimethyl-1-phenyl-, trans-
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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