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

Compound with spectra: 1 NMR

4-(BENZYLOXY)-5-ENDO-([(TERT.-BUTYLDIMETHYLSILYL)-OXY]-METHYL)-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE
SpectraBase Compound ID 9VdxsNhVTgb
InChI InChI=1S/C28H37NO5SSi/c1-21-12-14-25(15-13-21)35(31,32)29-24-16-17-28(26(29)30,33-19-22-10-8-7-9-11-22)23(18-24)20-34-36(5,6)27(2,3)4/h7-17,23-24H,18-20H2,1-6H3/t23-,24+,28+/m1/s1
InChIKey QSHKYXWBSFQZFW-NYULUDCUSA-N
Mol Weight 527.8 g/mol
Molecular Formula C28H37NO5SSi
Exact Mass 527.216171 g/mol
Enantiomer InChIKey QSHKYXWBSFQZFW-VYKTZEHYSA-N

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

13C NMR Spectrum
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Solvent CDCl3
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
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
4-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2-(4'-METHYLBENZENESULFONYL)-3-OXO-2-AZABICYCLO-[2.2.2]-OCT-7-ENE-5-ENDO-CARBOXALDEHYDE
4-([tert-Butyldimethylsilyl)oxy]-2-(4'-Methylbenzenesulfonyl)-3-oxo-2-azabicyclo[2.2.2]-7-octene-5-endo-carboxadehyde
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
Methyl (5S)-4-hydroxy-2-[(naphthalen-2'-yl)sulfonyl]-3-oxo-2-azabicyclo[2.2.2]oct-7-ene-5-carboxylate
3a,6-Ethano-3aH-indene-4-carboxylic acid, octahydro-1-hydroxy-5,5,7a-trimethyl-8-oxo-, ethyl ester, [1R-(1.alpha.,3a.alpha.,4.alpha.,6.al pha.,7a.alpha.)]-
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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