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(2S,6R,7R,8S)-8-SENECIOYLOXY-1(10),4,11(13)-GERMACRATRIEN-2,14,6,12-DIOLIDE

Compound with spectra: 3 NMR

(2S,6R,7R,8S)-8-SENECIOYLOXY-1(10),4,11(13)-GERMACRATRIEN-2,14,6,12-DIOLIDE
SpectraBase Compound ID AW8RT0w0g3B
InChI InChI=1S/C20H22O6/c1-10(2)5-17(21)25-16-9-13-8-14(24-20(13)23)6-11(3)7-15-18(16)12(4)19(22)26-15/h5,7-8,14-16,18H,4,6,9H2,1-3H3/b11-7+/t14-,15+,16-,18-/m0/s1
InChIKey OBWGPBQVBLCUCB-SWRBSBKJSA-N
Mol Weight 358.39 g/mol
Molecular Formula C20H22O6
Exact Mass 358.141638 g/mol
Enantiomer InChIKey OBWGPBQVBLCUCB-GAZBEUOASA-N

View Spectrum of (2S,6R,7R,8S)-8-SENECIOYLOXY-1(10),4,11(13)-GERMACRATRIEN-2,14,6,12-DIOLIDE

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

View Spectrum of (2S,6R,7R,8S)-8-SENECIOYLOXY-1(10),4,11(13)-GERMACRATRIEN-2,14,6,12-DIOLIDE

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

View Spectrum of (2S,6R,7R,8S)-8-SENECIOYLOXY-1(10),4,11(13)-GERMACRATRIEN-2,14,6,12-DIOLIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (2R,6R,7R,8S)-GERMACRA-1(10),4,11(13)-TRIEN-14,2;12,6-DIOLIDE,8-SENECIOYLOXY
  • (2S,6R,7R,8S)-GERMACRA-1(10),4,11(13)-TRIEN-12,6;14,2-DIOLIDE,8-SENECIOYLOXY
(2R,6R,7R,8S)-8-SENECIOYLOXY-1(10),4,11(13)-GERMACRATRIEN-2,14,6,12-DIOLIDE
DEOXYELEPHANTOPIN
2A,14-DIHYDROXY-8B-(2'R,3'R)-2',3'-EPOXYANGELOYLOXYCOSTUNOLIDE
KCUQHLKAVMLGGV-ACBQZUGDSA-N
Millisorin B
EUPTOLIDE,2-A-HYDROXY,8-(2S',3S'-EPOXYANGELATE)
EUPATOLIDE,2-A-HYDROXY,8-(2R',3R'-EPOXYANGELATE)=MOLLISORIN-B-A
COTUNOLIDE,2-A-HYDROXY-8-B-(2',3',5'-TRIHYDROXYANGELOYLOXIDE)
GERMACRA-1(10),4,11(13)-TRIEN-12,6-A-OLIDE,2-A-HYDROXY-8-B-(2',5'-DIHYDROXY-3'-MERCAPTO-2'-METHYLBUTANOYLOXY)
2-Hydroxy-2-(hydroxymethyl)-3-mercapto-2,3,3a,4,5,9,11a-octahydro-8-hydroxy-6,10-dimethyl-3-methylene-2-oxocyclodeca(b)furan-4-yl ester of (3aR-(3aR*,4R*(2S*,3S*),6E,8S*,10E,11aR*))-butanoic acid
Title Journal or Book Year
Deoxyelephantopin and 2-epideoxyelephantopin analogues from Gochnatia palosanto Phytochemistry 1990

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