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DIETHYL-2-[(1S,2S/R,5S)-6-TOSYL-3-THIA-6-AZABICYCLO-[3.2.1]-OCT-2-YL]-MALONATE;MAJOR-ISOMER

Compound with spectra: 2 NMR

DIETHYL-2-[(1S,2S/R,5S)-6-TOSYL-3-THIA-6-AZABICYCLO-[3.2.1]-OCT-2-YL]-MALONATE;MAJOR-ISOMER
SpectraBase Compound ID K5CgIOegyz6
InChI InChI=1S/2C20H27NO6S2/c2*1-4-26-19(22)17(20(23)27-5-2)18-14-10-15(12-28-18)21(11-14)29(24,25)16-8-6-13(3)7-9-16/h2*6-9,14-15,17-18H,4-5,10-12H2,1-3H3/t2*14-,15-,18+/m00/s1
InChIKey OHYHEOFOVIGNDT-MLGWWAEGSA-N
Mol Weight 883.11 g/mol
Molecular Formula C40H54N2O12S4
Exact Mass 882.25596 g/mol
Enantiomer InChIKey OHYHEOFOVIGNDT-ZIHZKTQHSA-N

View Spectrum of DIETHYL-2-[(1S,2S/R,5S)-6-TOSYL-3-THIA-6-AZABICYCLO-[3.2.1]-OCT-2-YL]-MALONATE;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of DIETHYL-2-[(1S,2S/R,5S)-6-TOSYL-3-THIA-6-AZABICYCLO-[3.2.1]-OCT-2-YL]-MALONATE;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • DIETHYL-2-[(1S,2S/R,5S)-6-TOSYL-3-THIA-6-AZABICYCLO-[3.2.1]-OCT-2-YL]-MALONATE;MINOR-ISOMER
7-Azabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 7-(p-tolylsulfonyl)-, dimethyl ester, trans-
(2S,3R,4S)-3-(N-Benzylamino)-2-(2-methylpropyl)-3-isopropenyl-N-tosylpiperidine
2-pyrrolidinecarboxylic acid, 1-[(4-methylphenyl)sulfonyl]-, (1R)-3-acetyl-4-hydroxy-2-oxo-3-cyclohexen-1-yl ester, (2S)-
(1S,5R)-8-Tosyl-2-((trimethylsilyl)ethynyl)-8-azabicyclo[3.2.1]octan-2-ol
cis-N-p-Toluenesulfonyl-3-(1,1-dimethyl-3-ethoxycarbonyl-3-buten-1-yl)-4-p-toluenesulfonylmethyl-pyrrolidine
cis-and trans-Ethyl 2-methyl-4-(phenylthio)-1-tosyl-1,2,5,6-tetrahydro-6-pyridinecarboxylate
(3S,6S)-1,6-DIBENZYL-3-METHYL-4-(PARA-TOLUENESULFONYL)-PIPERAZIN-2-ONE
(4as,7aS)-1,7-Dimethyl-4-oxo-6-tosyloctahydro-1H-pyrrolo[3,4-b]pyridine
(2SR,4S,5S)-5-{[(tert-Butyldiphenylsilyl)oxy]methyl}-1-tosyl-4-[4-(trimethylsilyl)but-3-ynyl]pyrrolidin-2-ol
7-Acetoxy-4-(4'-chlorophenylsulphonyl)-4-azatetracyclo[3.3.0.0(2,8).0(3,6)]octane
Title Journal or Book Year
Efficient Stereoselective Alkenylation through a Homolytic Domino Reaction Involving a 1,5 Sulfur-to-Carbon Translocation Journal of the American Chemical Society 2004
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