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(-)-1-[(1'S,4'R)-Camphanoyl]-(R)-spirobrassinin

Compound with spectra: 2 NMR, and 2 MS (GC)

(-)-1-[(1'S,4'R)-Camphanoyl]-(R)-spirobrassinin
SpectraBase Compound ID DxUntxUCN5D
InChI InChI=1S/C21H22N2O4S2/c1-18(2)19(3)9-10-21(18,27-16(19)26)15(25)23-13-8-6-5-7-12(13)20(14(23)24)11-22-17(28-4)29-20/h5-8H,9-11H2,1-4H3/t19-,20-,21+/m0/s1
InChIKey SHYMUJCIPQMRMM-PCCBWWKXSA-N
Mol Weight 430.54 g/mol
Molecular Formula C21H22N2O4S2
Exact Mass 430.1021 g/mol
Enantiomer InChIKey SHYMUJCIPQMRMM-NJYVYQBISA-N

View Spectrum of (-)-1-[(1'S,4'R)-Camphanoyl]-(R)-spirobrassinin

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum C4-2000-887-6

View Spectrum of (-)-1-[(1'S,4'R)-Camphanoyl]-(R)-spirobrassinin

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-66-3947-19

View Spectrum of (-)-1-[(1'S,4'R)-Camphanoyl]-(R)-spirobrassinin

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

View Spectrum of (-)-1-[(1'S,4'R)-Camphanoyl]-(R)-spirobrassinin

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (-)-1-[(1'S,4'R)-Camphanoyl]-(S)-spirobrassinin
Title Journal or Book Year
Synthesis, Absolute Configuration, and Enantiomeric Enrichment of a Cruciferous Oxindole Phytoalexin, (S)-(−)-Spirobrassinin, and Its Oxazoline Analog The Journal of Organic Chemistry 2001
(-)-1-[(1'S,4'R)-Camphanoyl]-(S)-spirobrassinin
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