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METHYL-(S*)-4-IODO-4-(R*)-4-METHOXY-8-OXO-2,3,6,8-TETRAHYDRO-1H-FURO-[3,4-G]-BENZOFURAN-2-YL]-PENTANOATE

Compound with spectra: 1 NMR

METHYL-(S*)-4-IODO-4-(R*)-4-METHOXY-8-OXO-2,3,6,8-TETRAHYDRO-1H-FURO-[3,4-G]-BENZOFURAN-2-YL]-PENTANOATE
SpectraBase Compound ID AY1gP7J6f18
InChI InChI=1S/C17H19IO6/c1-17(18,5-4-13(19)22-3)12-7-10-11(21-2)6-9-8-23-16(20)14(9)15(10)24-12/h6,12H,4-5,7-8H2,1-3H3/t12-,17+/m0/s1
InChIKey ZJDDLEHMPISQDE-YVEFUNNKSA-N
Mol Weight 446.24 g/mol
Molecular Formula C17H19IO6
Exact Mass 446.022633 g/mol
Enantiomer InChIKey ZJDDLEHMPISQDE-PXAZEXFGSA-N

View Spectrum of METHYL-(S*)-4-IODO-4-(R*)-4-METHOXY-8-OXO-2,3,6,8-TETRAHYDRO-1H-FURO-[3,4-G]-BENZOFURAN-2-YL]-PENTANOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
10H-Isobenzofuro[5,6-b][1,4]benzodioxepin-3,10(1H)-dione,4,7-dimethoxy-9-methyl-
10H-Isobenzofuro[5,6-b][1,4]benzodioxepin-3,10(1H)-dione, 7-hydroxy-4-methoxy-9-methyl-
Phellodensin-C
3,5',7'-trihydroxy-4-methoxyspiro[bicyclo[4.2.0]octa-1,3,5-triene-8,3'-chroman]-4'-one
1,7-DIHYDROXY-2,3-[2''-(1-HYDROXY-1-METHYLETHYL)-DIHYDROFURANO]-XANTHONE
11H-Dibenzo[b,e][1,4]dioxepin-7-carboxylic acid, 8-hydroxy-3-methoxy-1,4,6,9-tetramethyl-11-oxo-, methyl ester
5-HYDROXYMETHYL-4,4,8-TRIMETHYLANTHRACEN-1,9,10(4H)-TRIONE
EXIGUAFLAVANONE-E;(2S)-5,2',4'-TRIHYDROXY-8-LAVANDULYL-7,5'-DIMETHOXY-FLAVANONE
EXIGUAFLAVANONE E ; (2S)-5,2',4'-TRIHYDROXY-8-LAVAVDULYL-7,5'-DIMETHOXYFLAVANONE
5,10-Epoxy-5H-dibenzo[a,d]cycloheptene, 10,11-dihydro-5,10-diphenyl-
Title Journal or Book Year
Total Synthesis of Mycophenolic Acid by a Palladium-Catalyzed Decarboxylative Allylation and Biomimetic Aromatization Sequence European Journal of Organic Chemistry 2013
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