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(7E,1S,3S,4R,12S,13R,14R)-13-ACETOXY-3,4-EPOXY-CEMBRA-7,15-DIEN-16,14-OLIDE,EUPALMERIN-ACETATE

Compound with spectra: 1 NMR

(7E,1S,3S,4R,12S,13R,14R)-13-ACETOXY-3,4-EPOXY-CEMBRA-7,15-DIEN-16,14-OLIDE,EUPALMERIN-ACETATE
SpectraBase Compound ID 1FbXGRlyWyq
InChI InChI=1S/C22H32O5/c1-13-8-6-10-14(2)19(25-16(4)23)20-17(15(3)21(24)26-20)12-18-22(5,27-18)11-7-9-13/h9,14,17-20H,3,6-8,10-12H2,1-2,4-5H3/b13-9-/t14-,17-,18-,19-,20+,22+/m1/s1
InChIKey KSMMWIWWLQEPOL-IDTHGUSQSA-N
Mol Weight 376.5 g/mol
Molecular Formula C22H32O5
Exact Mass 376.224974 g/mol
Enantiomer InChIKey KSMMWIWWLQEPOL-TZUJLDPPSA-N

View Spectrum of (7E,1S,3S,4R,12S,13R,14R)-13-ACETOXY-3,4-EPOXY-CEMBRA-7,15-DIEN-16,14-OLIDE,EUPALMERIN-ACETATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
No Name
12,13-bis[epi]-Eupalmerin - Acetate
12-epi-Eupalmerin-Acetate
12,13-bis[epi]-Eupalmerin - Acetate
12-epi-Eupalmerin-Acetate
20-ACETYLSINULAROLIDE_B
(7E,11E)-18-ACETOXY-3,4-EPOXY-13-HYDROXY-7,11,15(17)-CEBRATRIEN-16,14-OLIDE
20-ACETYLSINULAROLIDE_C
CRASSOCOLIDE_A;(1-R,3-S,4-R,13-S,14-R,7-E,11-E)-13-ACETOXY-3,4-DIHYDROXYCEMBRA-7,11,15-(17)-TRIEN-16,14-OLIDE
4,14-Eupalmeroic acid
2-[(1S,4E,9S,10S,11R,12S,14R)-10,14-dihydroxy-1,5,9-trimethyl-15-oxabicyclo[9.3.1]pentadec-4-en-12-yl]acrylic acid
methyl (Z)-2-[(1R,2S,3R,7E,11R,12S,14S)-2,11-dihydroxy-3,7,11-trimethyl-15-oxabicyclo[10.2.1]pentadec-7-en-14-yl]but-2-enoate
methyl (E)-2-[(1R,2S,3R,7E,11R,12S,14S)-2,11-dihydroxy-3,7,11-trimethyl-15-oxabicyclo[10.2.1]pentadec-7-en-14-yl]but-2-enoate
UPROLIDE-K-ACETATE
Title Journal or Book Year
Application of two-dimensional NMR spectroscopy in the structural determination of marine natural products. Total structural assignment of the cembranoid diterpene eupalmerin acetate through the use of two-dimensional proton-proton, proton-carbon-13, and carbon-13-carbon-13 chemical shift correlation spectroscopy The Journal of Organic Chemistry 1990

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