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PALMARUMYCIN-C2;2,3-EPOXY-2,3-DIHYDRO-5-HYDROXYSPIRO-[NAPHTHALENE-1(4H),2'-NAPHTHO-[1,8-DE]-[1,3]-DIOXIN]-4-ONE

Compound with spectra: 1 NMR, and 2 MS (GC)

PALMARUMYCIN-C2;2,3-EPOXY-2,3-DIHYDRO-5-HYDROXYSPIRO-[NAPHTHALENE-1(4H),2'-NAPHTHO-[1,8-DE]-[1,3]-DIOXIN]-4-ONE
SpectraBase Compound ID 7r86gxNDH5M
InChI InChI=1S/C20H12O5/c21-12-7-3-6-11-16(12)17(22)18-19(23-18)20(11)24-13-8-1-4-10-5-2-9-14(25-20)15(10)13/h1-9,18-19,21H
InChIKey QVLQAXXFMIVMPV-UHFFFAOYSA-N
Mol Weight 332.31 g/mol
Molecular Formula C20H12O5
Exact Mass 332.068473 g/mol

View Spectrum of PALMARUMYCIN-C2;2,3-EPOXY-2,3-DIHYDRO-5-HYDROXYSPIRO-[NAPHTHALENE-1(4H),2'-NAPHTHO-[1,8-DE]-[1,3]-DIOXIN]-4-ONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum U-1994-1105-2

View Spectrum of PALMARUMYCIN-C2;2,3-EPOXY-2,3-DIHYDRO-5-HYDROXYSPIRO-[NAPHTHALENE-1(4H),2'-NAPHTHO-[1,8-DE]-[1,3]-DIOXIN]-4-ONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F-57-293-0

View Spectrum of PALMARUMYCIN-C2;2,3-EPOXY-2,3-DIHYDRO-5-HYDROXYSPIRO-[NAPHTHALENE-1(4H),2'-NAPHTHO-[1,8-DE]-[1,3]-DIOXIN]-4-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (+-)-2,3-Epoxy-8-hydroxy-1,2,3,4-tetrahydronaphthalene-4-spiro-2'-naphtho[1",8"-de][1',3']-dioxin
Deoxypreussomerin A
5-Methoxyspiro[tetrahydro-2,3-dihydroxynaphthalene-1,2'-naphtho[1,8-de][1,3]dioxin]-4-one
Palmarumycin C11
PALMARUMYCIN-JC1
PALMARUMYCIN-C11;2,3-EPOXY-4,5-DIHYDROXY-1,2,3,4-TETRAHYDROSPIRO-[NAPHTHALENE-1,2'-NAPHTHO-[1,8-DE]-[1,3]-DIOXINE]
5-O-METHYL-PALMARUMYCIN-C2
Palmarumycin BG5
Palmarumycin BG6
MPC1001H
Diethyl (1R,3R,7aR)-1-methyl-1,3-diphenyl-4-(1-phenylvinyl)-3,5,7,7a-tetrahydrocyclopenta[c]pyran-6,6(1H)-dicarboxylate
Title Journal or Book Year
The synthesis of 1,8-dihydroxynaphthalene-derived natural products: palmarumycin CP1, palmarumycin CP2, palmarumycin C11, CJ-12,371, deoxypreussomerin A and novel analogues Journal of the Chemical Society, Perkin Transactions 1 1999
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