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(+)-11-BETA,13-DIHYDROREYNOSIN

Compound with spectra: 6 NMR

(+)-11-BETA,13-DIHYDROREYNOSIN
SpectraBase Compound ID 2rZBIJ6KEy
InChI InChI=1S/C15H22O3/c1-8-4-5-11(16)15(3)7-6-10-9(2)14(17)18-13(10)12(8)15/h9-13,16H,1,4-7H2,2-3H3/t9-,10-,11+,12+,13-,15-/m0/s1
InChIKey JWBPWNWPEVPCMJ-DMLGPZFASA-N
Mol Weight 250.34 g/mol
Molecular Formula C15H22O3
Exact Mass 250.156895 g/mol
Enantiomer InChIKey JWBPWNWPEVPCMJ-CDWXYHGHSA-N

View Spectrum of (+)-11-BETA,13-DIHYDROREYNOSIN

13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Chloroform

View Spectrum of (+)-11-BETA,13-DIHYDROREYNOSIN

13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Chloroform

View Spectrum of (+)-11-BETA,13-DIHYDROREYNOSIN

13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Chloroform

View Spectrum of (+)-11-BETA,13-DIHYDROREYNOSIN

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

View Spectrum of (+)-11-BETA,13-DIHYDROREYNOSIN

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

View Spectrum of (+)-11-BETA,13-DIHYDROREYNOSIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (11S)-1-BETA-HYDROXYEUDESM-4(14)-ENO-13,6-ALPHA-LACTONE
  • 1-BETA-HYDROXY-5,7-ALPHA-H,6,11-BETA-H-EUDESM-4-(15)-EN-6,12-OLIDE
  • REYNOSIN, 11-beta,13-DIHYDRYL-A
  • REYNOSIN,11-B,13-DIHYDRO-B
  • REYNOSIN,11-B,13-DIHYDRO-C
SESQUITERPENE LP-I
1alpha-HYDROXYEUDESM-4(15)-EN-5alpha,6beta,11betaH-12,6-OLIDE
11-BETA,13-DIHYDRO-1-EPIREYNOSIN;1-ALPHA-HYDROXYEUDESM-4(15)-EN-5-ALPHA,6-BETA,11-BETA-H-12,6-OLIDE
11-EPI-DIHYDRO-REYNOSIN
REYNOSIN,11-A,13-DIHYDRO
(3S,3aS,5aS,6S,9aR,9bR)-6-hydroxy-3,5a-dimethyl-9-methylidene-3a,4,5,6,7,8,9a,9b-octahydro-3H-naphtho[3,4-d]furan-2-one
DIHYDRO-REYNOSIN
1-BETA-HYDROXY-4-OXO-11-BETA-H-4-NOREUDESMAN-6,12-OLIDE
1,2-BETA-EPOXY-5,7-ALPHA-H,6,11-BETA-H-ELEM-3-EN-6,12-OLIDE
(E)-4-hydroxy-4-methyl-pent-2-enoic acid [(1S,2R,4aS,5S,8aR)-2-acetyl-5-hydroxy-4a-methyl-8-methylene-decalin-1-yl] ester
Title Journal or Book Year
Effects of Solvents and Water in Ti(III)-Mediated Radical Cyclizations of Epoxygermacrolides. Straightforward Synthesis and Absolute Stereochemistry of (+)-3α-Hydroxyreynosin and Related Eudesmanolides The Journal of Organic Chemistry 2002
Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives Journal of Natural Products 1998
Synthesis of torrentin, dihydrosantamarine, and saussurea lactone from santonin Canadian Journal of Chemistry 1992
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