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#6;[2A-R-(4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-2A,3,4,4A,5,6,7A,7B-OCTAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE

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

#6;[2A-R-(4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-2A,3,4,4A,5,6,7A,7B-OCTAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE
SpectraBase Compound ID YnMGWIl8Ig
InChI InChI=1S/C10H16O5/c11-2-6-9(13)8-5(12)1-4-3-14-10(15-6)7(4)8/h4-13H,1-3H2/t4-,5-,6+,7+,8-,9+,10-/m0/s1
InChIKey IZKUEBAEZIXDEC-SGWQGHRUSA-N
Mol Weight 216.23 g/mol
Molecular Formula C10H16O5
Exact Mass 216.099774 g/mol
Enantiomer InChIKey IZKUEBAEZIXDEC-BGJVCVCZSA-N

View Spectrum of #6;[2A-R-(4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-2A,3,4,4A,5,6,7A,7B-OCTAHYDRO-4,5-DIHYDROXY-6-[(HYDROXY)-METHYL]-2H-1,7-DIOXACYCLOPENT-[CD]-INDENE

MS (GC) Spectrum
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Source of Spectrum J-64-8308-6

View Spectrum of #6;[2A-R-(4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA,7B-BETA)]-2A,3,4,4A,5,6,7A,7B-OCTAHYDRO-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
  • [2aR-(4.beta.,4a.alpha.,5.beta.,6.alpha.,7a.alpha.,7b.alpha.)]-2a,3,4,4a,5,6,7a,7b-Octahydro-4,5-(dihydroxy)-6-[(hydroxy)methyl]-2H-1,7-dioxacyclopent[cd]indene
3-O-ALLOSYL-EPOXY-CERBERIDOL
4.beta.,10.beta.-Di-n-butyl-3,11-dioxatetracyclo[6.3.0.0(2,6).0(5,9)]undecane
(1S,2S,4R)-PARA-MENTHANE-1,2,8-TRIOL-2-O-BETA-D-GLUCOPYRANOSIDE
Methyl 5,6-isopropylidene-2,3-([2R]-hydroxy-propane-1,3-diyl)-2,3-dideoxy-A,B-D-talofuranoside
NINGPOGOSIDE B
NINGPOGOSIDE-B;REL-(1R,5R,6R)-(6-(GLUCOSYLOXYMETHYL)-2-OXA-BICYCLO-[3.3.0]-OCT-7-EN-7-YL)-METHANOL
3,6-ENDO,ENDO-DIHYDROXY-2,7-OXATETRACYCLO[6.3.0.0(4,11).0(5,9)]UNDECANE
2-(TETRADECYL)-HEXADECYL-O-(BETA-D-GALACTOPYRANOSYL)-(1->4)-BETA-D-GLUCOPYRANOSIDE
ZIZYBEOSIDE-I;PHENETHYL-ALCOHOL-8-O-BETA-D-GLUCOPYRANOSYL-(1->2)-BETA-D-GLUCOPYRANOSIDE
Mannopyranosyl-A-(1->2)-mannopyranosyl-A-(1->6)-residue
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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