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4-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE

Compound with spectra: 1 NMR

4-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE
SpectraBase Compound ID GlOeSawkegi
InChI InChI=1S/C21H29NO5SSi/c1-15-7-9-18(10-8-15)28(25,26)22-17-11-12-21(19(22)24,16(13-17)14-23)27-29(5,6)20(2,3)4/h7-12,14,16-17H,13H2,1-6H3/t16-,17+,21+/m1/s1
InChIKey UTQDEMYOOHOSNG-WWMYMODYSA-N
Mol Weight 435.61 g/mol
Molecular Formula C21H29NO5SSi
Exact Mass 435.153571 g/mol
Enantiomer InChIKey UTQDEMYOOHOSNG-CSODHUTKSA-N

View Spectrum of 4-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
4-([tert-Butyldimethylsilyl)oxy]-2-(4'-Methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene-5-endo-carboxadehyde
4-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-5-ENDO-(HYDROXYMETHYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
Methyl 4-Methoxy-2-(4'-Methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-endo-carboxylate
5-endo-[[(Butyldimethylsilyl)oxy]methyl]-4-(4"-Methylbenzenesulfenyl)-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene
4-(Benzyloxy)-5-endo-[(tert-butyldimethylsilyloxy)methyl]-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene
4-(BENZYLOXY)-5-ENDO-([(TERT.-BUTYLDIMETHYLSILYL)-OXY]-METHYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
Methyl (5S)-4-hydroxy-2-[(naphthalen-2'-yl)sulfonyl]-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-carboxylate
Methyl (5R)-4-hydroxy-2-[(naphthalen-2'-yl)sulfonyl]-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-carboxylate
(1R,4R,5S)-methyl 4-hydroxy-2-(naphthalen-2-ylsulfonyl)-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-carboxylate
7-Allyl-2-[(4-methylphenyl)sulfonyl]-4-nitro-2,11-dihydro[1]benzoxepino[4,3,2-cd]indole
XYLARENAL-B
Title Journal or Book Year
Diels-Alder cycloadditions using nucleophilic 2-pyridones. Regiocontrolled and stereocontrolled synthesis of unsaturated, bridged, bicyclic lactams The Journal of Organic Chemistry 1992
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