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(+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE

Compound with spectra: 2 NMR, and 3 MS (GC)

(+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE
SpectraBase Compound ID Cj0ayijbtqL
InChI InChI=1S/C7H12O4/c1-3-2-4(8)6(10)7(11)5(3)9/h3-4,6-8,10-11H,2H2,1H3
InChIKey FQFXYFNHFVFHPV-UHFFFAOYSA-N
Mol Weight 160.17 g/mol
Molecular Formula C7H12O4
Exact Mass 160.073559 g/mol

View Spectrum of (+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum U-1993-248-6

View Spectrum of (+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum U-1993-247-2

View Spectrum of (+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum H-69-1831-1

View Spectrum of (+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of (+/-)-EPIGABOSINE-O;(2RS,3RS,4SR,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • (+/-)-GABOSINE-O;(2RS,3RS,4RS,6SR)-2,3,4-TRIHYDROXY-6-METHYLCYCLOHEXANONE
  • 2,3,4-Trihydroxy-6-methylcyclohexanone
1-O-Acetylfructose
D-MANNOHEPTULOSE
Hept-2-ulose
(+-)-[(2R,3S)-3-(Hydroxymethyl)oxiran-2-yl](cyclohexyl)methanone
D-ARABINOAMIDE-5-PHOSPHATE
(2S,4S,5S)-2-chloro-4,5-dihydroxy-6-keto-6-methoxy-hexanoic acid
Methyl-trans-3,4-dihydroxycyclohexanecarboxylate
Methyl-cis-3,4-dihydroxycyclohexanecarboxycylate
1,2-Dicyclohexyl-2-oxidanyl-ethanone
Arabinonic acid, calcium salt (2:1)
Title Journal or Book Year
Enantioselective Synthesis and Absolute Configuration Assignment of Gabosine O. Synthesis of (+)- and (−)-Gabosine N and (+)- and (−)-Epigabosines N and O Organic Letters 2006
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