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4-(4''-METHYLBENZENESULFENYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE

Compound with spectra: 1 NMR

4-(4''-METHYLBENZENESULFENYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE
SpectraBase Compound ID 32evJb9GP92
InChI InChI=1S/C22H21NO4S2/c1-15-3-7-19(8-4-15)28-22-12-11-18(13-17(22)14-24)23(21(22)25)29(26,27)20-9-5-16(2)6-10-20/h3-12,14,17-18H,13H2,1-2H3/t17-,18+,22+/m1/s1
InChIKey XAQGHRWHENPWEV-FGSXEWAUSA-N
Mol Weight 427.53 g/mol
Molecular Formula C22H21NO4S2
Exact Mass 427.091201 g/mol
Enantiomer InChIKey XAQGHRWHENPWEV-NJNPRVFISA-N

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

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
4-(4"-Methylbenzenesulfenyl)-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene-5-endo-carboxaldehyde
5-ENDO-(HYDROXYMETHYL)-4-(4''-METHYLBENZENESULFENYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
4-(4''-METHYLBENZENESULFENYL)-2-(4'-METHYLBENZENESULFONYL)-5-ENDO-NITRO-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
4-([tert-Butyldimethylsilyl)oxy]-2-(4'-Methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene-5-endo-carboxadehyde
4-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE
Methyl 4-Methoxy-2-(4'-Methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-endo-carboxylate
4-(BENZYLOXY)-5-ENDO-([(TERT.-BUTYLDIMETHYLSILYL)-OXY]-METHYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
4-(Benzyloxy)-5-endo-[(tert-butyldimethylsilyloxy)methyl]-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene
4-(BENZYLOXY)-2-(4'-METHYLBENZENESULFONYL)-5-ENDO-NITRO-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
ZN(II)-L1
ERIOCASIN_C;19-ACETOXY-3-BETA,6-BETA-DIHYDROXY-7,16-DIOXO-ENT-ABIETA-15-(17)-ENE
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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