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11-BETA,13-DIHYDRO-LUDARTIN

Compound with spectra: 1 NMR

11-BETA,13-DIHYDRO-LUDARTIN
SpectraBase Compound ID 4KBnfhztJ63
InChI InChI=1S/C15H20O3/c1-7-4-5-9-8(2)14(16)17-13(9)12-10(7)6-11-15(12,3)18-11/h8-9,11-13H,4-6H2,1-3H3/t8-,9?,11+,12-,13-,15+/m0/s1
InChIKey WLJBKCYEKTZMBW-GDGHXFNASA-N
Mol Weight 248.32 g/mol
Molecular Formula C15H20O3
Exact Mass 248.141245 g/mol
Enantiomer InChIKey WLJBKCYEKTZMBW-SEQUPLTPSA-N

View Spectrum of 11-BETA,13-DIHYDRO-LUDARTIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
3,4-epoxyguai-1(10)-en-6,12-olide
LUDARTIN,11-B,13-DIHYDRO
(11S)-3-BETA,4-BETA-EPOXY-GUAIA-1(10)-ENO-12,6-ALPHA-LACTONE
(3S,4R,5R,6S,7S,11S)-GUAI-1(10)-EN-12,6-OLIDE,3,4-EPOXY
Naphtho[1,2-b]furan-2(3H)-one, 5,6-bis(acetyloxy)decahydro-3,5a-dimethyl-9-methylene-, [3S-(3.alpha.,3a.alpha.,5.beta.,5a.beta.,6.beta.,9a.alpha.,9b.beta.)]-
11-ALPHA,13-DIHYDROGLUCOZALUZANIN-C
1.alpha.,13-Dichloro-10.beta.-hydroxyarglabin
(11S,16R)-11,16-Epoxy-13-ethylmokkolactone
(11R,16R)-11,16-Epoxy-13-ethylmokkolactone
16.alpha.,17-Dihydroxyjungermannenone A
Title Journal or Book Year
Studies on the Synthesis of Sesquiterpene Lactones, 16. The Syntheses of 11β,13-Dihydrokauniolide, Estafiatin, Isodehydrocostuslactone, 2-Oxodesoxyligustrin, Arborescin, 1,10-Epiarborescin, 11β,13-Dihydroludartin, 8-Deoxy-11β,13-dihydrorupicolin B, 8-Deoxyrupicolin B, 3,4-Epiludartin, Ludartin, Kauniolide, Dehydroleucodin, and Leucodin Journal of Natural Products 1994

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