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(2S,4R)-1-(4-METHYLPHENYLSULFONYL)-4-[(E)-2-PHENYL-1-ETHENYL]-2-[(E)-2-PHENYL-1-ETHENYLSULFINYLMETHYL]-PYRROLIDINE;LESS-POLAR-ISOMER

Compound with spectra: 2 NMR

(2S,4R)-1-(4-METHYLPHENYLSULFONYL)-4-[(E)-2-PHENYL-1-ETHENYL]-2-[(E)-2-PHENYL-1-ETHENYLSULFINYLMETHYL]-PYRROLIDINE;LESS-POLAR-ISOMER
SpectraBase Compound ID 7OIsJUow1qg
InChI InChI=1S/C28H29NO3S2/c1-23-12-16-28(17-13-23)34(31,32)29-21-26(15-14-24-8-4-2-5-9-24)20-27(29)22-33(30)19-18-25-10-6-3-7-11-25/h2-19,26-27H,20-22H2,1H3/b15-14+,19-18+/t26-,27-,33?/m0/s1
InChIKey ZDDVKYZRZPRGBT-JZYIOJRVSA-N
Mol Weight 491.66 g/mol
Molecular Formula C28H29NO3S2
Exact Mass 491.158886 g/mol
Enantiomer InChIKey ZDDVKYZRZPRGBT-PUIDZNNVSA-N

View Spectrum of (2S,4R)-1-(4-METHYLPHENYLSULFONYL)-4-[(E)-2-PHENYL-1-ETHENYL]-2-[(E)-2-PHENYL-1-ETHENYLSULFINYLMETHYL]-PYRROLIDINE;LESS-POLAR-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 (2S,4R)-1-(4-METHYLPHENYLSULFONYL)-4-[(E)-2-PHENYL-1-ETHENYL]-2-[(E)-2-PHENYL-1-ETHENYLSULFINYLMETHYL]-PYRROLIDINE;LESS-POLAR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (2S,4R)-1-(4-METHYLPHENYLSULFONYL)-4-[(E)-2-PHENYL-1-ETHENYL]-2-[(E)-2-PHENYL-1-ETHENYLSULFINYLMETHYL]-PYRROLIDINE;MORE-POLAR-ISOMER
(E)-(2S,4R)-4-[2,2-BIS-(ETHOXYCARBONYL)-ETHENYL]-1-(4-METHYLPHENYLSULFONYL)-2-[(E)-2-PHENYL-1-ETHENYLSULFANYLMETHYL]-PYRROLIDINE;MAJOR-ISOMER
(Z)-(2S,4R)-4-[2,2-BIS-(ETHOXYCARBONYL)-ETHENYL]-1-(4-METHYLPHENYLSULFONYL)-2-[(Z)-2-PHENYL-1-ETHENYLSULFANYLMETHYL]-PYRROLIDINE;MINOR-ISOMER
1-(4'-Methylphenylsulfonyl)-1-aza-3-methylenebicyclo[4.3.0]nona-5-ene
(E)-and (Z)-2-[(2-Ethoxycarbonyl)ethenyl]-4-(phenylthio)-1-toluenesulfonyl-1,2,3,6-tetrahydropyridine
(E)-2-cyano-4-[(4Z)-1-(4-methylphenyl)sulfonyl-4-(phenylmethylene)-3-pyrrolidinyl]-2-butenoic acid methyl ester
2-Pyrrolidineacetic acid, .alpha.,4,4-trimethyl-1-[(4-methylphenyl)sulfonyl]-, methyl ester, (R*,S*)-(.+-.)-
N-Tolysulfonyl-2S-(1R-methoxycarbonyl-ethyl)-4,4-dimethyl-pyrrolidine
5-(N-Allyl-N-tosylamino)-3-(tert-butyldimethylsiloxy)cyclohept-6-en-1-ol
N-[4-[2-(Trimethylsilyl)ethyl]-3-tosylthiazolidin-2-ylidene]benzenamine
N-((2,3-Diphenylcycloallyl)methyl)-4-methyl-N-(4-phenylbut-3-yn-2-yl)benzenesulfonamide
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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