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2-DESOXY-11-BETA,13-DIHYDRO-EPIPARTHEMOLLIN

Compound with spectra: 2 NMR

2-DESOXY-11-BETA,13-DIHYDRO-EPIPARTHEMOLLIN
SpectraBase Compound ID 6LWSiSBk8jN
InChI InChI=1S/C15H22O3/c1-9-4-7-13-11(3)15(17)18-14(13)8-12(9)6-5-10(2)16/h8-9,11,13-14H,4-7H2,1-3H3/t9-,11-,13-,14+/m0/s1
InChIKey YMEVSAAYOZFKIF-DTCNJJKHSA-N
Mol Weight 250.34 g/mol
Molecular Formula C15H22O3
Exact Mass 250.156895 g/mol
Enantiomer InChIKey YMEVSAAYOZFKIF-IMJCEVDSSA-N

View Spectrum of 2-DESOXY-11-BETA,13-DIHYDRO-EPIPARTHEMOLLIN

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

View Spectrum of 2-DESOXY-11-BETA,13-DIHYDRO-EPIPARTHEMOLLIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • PARTHEMOLLIN,6-EPI,2-DESOXY-11-B,13-DIHYDRO
2-Deoxy-11.beta.-13-dihydro-6-(epi)-partenolide
GALLICIN,ACETATE-A
LACTULIDE A
11-B-H-GERMACRA-1(10)E,4E-DIEN-12,6-A-OLIDE,3-B,14-DIHYDROXY
SHONACALIN S
SHONACHALIN C
GSLRFQSAMMVDEI-YDHNIYMWSA-N
(3R,3aR,4R,6E,10E,11aS)-4-hydroxy-3,6,10-trimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[d]furan-2-one
BALCHANOLIDE
KETOPELENOLIDE_C
Title Journal or Book Year
Biomimetic Transformations of 11,13-Dihydroparthenolide and Oxidative Rearrangements ofa Guai- 1(10)-en-6,12-olide Journal of Natural Products 1989

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