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[4-S-(4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-4,4A,5,6,7A,7B-HEXAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE

Compound with spectra: 1 NMR, and 1 MS (GC)

[4-S-(4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-4,4A,5,6,7A,7B-HEXAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE
SpectraBase Compound ID DiyYXu5qo17
InChI InChI=1S/C10H14O5/c11-2-6-9(13)8-5(12)1-4-3-14-10(15-6)7(4)8/h1,5-13H,2-3H2/t5-,6+,7+,8-,9+,10-/m0/s1
InChIKey QNUDUBFDUZCLJD-DLXYEPTOSA-N
Mol Weight 214.22 g/mol
Molecular Formula C10H14O5
Exact Mass 214.084124 g/mol
Enantiomer InChIKey QNUDUBFDUZCLJD-TUUAOYNMSA-N

View Spectrum of [4-S-(4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-4,4A,5,6,7A,7B-HEXAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-64-8309-8

View Spectrum of [4-S-(4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-4,4A,5,6,7A,7B-HEXAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • [4S-(4a.alpha.,5.alpha.,6.beta.,7a.alpha.,7b.alpha.)]-4,5-(Dihydroxy)-6-[(hydroxy)methyl]-4,4a,5,6,7a,7b-hexahydro-2H-1,7-dioxacyclopent[cd]indene
PATRINOVALEROSIDATE;1-O-ISOVALEROXYL-11-O-BETA-D-GLUCOPYRANOSYL-JATAMANIN-J
REL-(1S,2R,3R)-TERPINOLENE-1,2,3-TRIOL-3-O-BETA-D-GLUCOPYRANOSIDE
IXERIN I
LOASASIDE
DEMETHYLSECOLOGANOL
3-Glucosyl-germacradigenolide
TURPINIONOSIDE-D;(3S,4R,9R)-3,4,9-TRIHYDROXY-MEGASTIGMAN-5-ENE-3-O-BETA-D-GLUCOPYRANOSIDE
(8S)-7,8-DIHYDRO-AUCUBIN
BALIBALOSIDE
METHYL-3-O-BENZYL-4,6-O-BENZYLIDENE-2-DEOXY-2-C-(PROP-2-ENYL)-ALPHA-D-ALTROSIDE
Title Journal or Book Year
Iridoids from Carbohydrates via Pauson−Khand Reaction:  Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from d-Glucal Derivatives The Journal of Organic Chemistry 1999
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