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(-)-(2R,3S,4R)-2-(4'-HYDROXYBENZYL)-3-[3'',4''-DIMETHOXYPHENYL)-(HYDROXY)-METHYL)]-4-(METHYLOXY)-BUTYROLACTONE

Compound with spectra: 2 NMR

(-)-(2R,3S,4R)-2-(4'-HYDROXYBENZYL)-3-[3'',4''-DIMETHOXYPHENYL)-(HYDROXY)-METHYL)]-4-(METHYLOXY)-BUTYROLACTONE
SpectraBase Compound ID 4g15ebcYxjM
InChI InChI=1S/C30H40O7/c1-17(2)22-12-6-18(3)14-25(22)36-30-27(28(32)20-9-13-24(34-4)26(16-20)35-5)23(29(33)37-30)15-19-7-10-21(31)11-8-19/h7-11,13,16-18,22-23,25,27-28,30-32H,6,12,14-15H2,1-5H3/t18?,22?,23-,25?,27+,28?,30-/m1/s1
InChIKey MUDNGZUGQHBYRN-PXYDJUTQSA-N
Mol Weight 512.6 g/mol
Molecular Formula C30H40O7
Exact Mass 512.277404 g/mol
Enantiomer InChIKey MUDNGZUGQHBYRN-YVUVPGCWSA-N

View Spectrum of (-)-(2R,3S,4R)-2-(4'-HYDROXYBENZYL)-3-[3'',4''-DIMETHOXYPHENYL)-(HYDROXY)-METHYL)]-4-(METHYLOXY)-BUTYROLACTONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (-)-(2R,3S,4R)-2-(4'-HYDROXYBENZYL)-3-[3'',4''-DIMETHOXYPHENYL)-(HYDROXY)-METHYL)]-4-(METHYLOXY)-BUTYROLACTONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(-)-(3S,4R,5R,6R)-3-(3',4'-Dimethoxy-.alpha.-hydroxybenzyl)-4-(3",4"-dimethoxybenzyl)-5-(1-menthyloxy)butyrolactone
allo-Hydroxymatairesinol-4-O-.alpha.-L-rhamnoside
(7'S,8S,8'R)-3,3',4,4'-bis(Methylenedioxy)-8'-[(3'',5''-dinitrobenzoyloxy)methyl]lignano-9,7'-lactone
2(S*)-[.alpha.(S*)-Acetoxy-3,4-dimethoxybenzyl]-3(S*)-[.alpha.(R*)-3,4-(methylenedioxy)benzyl]butyrolactone
Haplotonin
(+)-DE-4''-O-METHYLMAGNOLIN-4''-O-BETA-D-GLUCOPYRANOSIDE
(+)-Pinoresinol monomethyl ether B-D-glucoside
(2S,3R,4R)-2-(3',4'-Dimethoxyphenyl)-4-{[4'-(.beta.-D-glucopyranosyloxy)-3'-methoxyphenyl]methyl}tetrahydrofuran-3-methanol
(2R,3R,4S)-4-(3',4'-Dimethoxybenzoyl)-2-(3",4"-methylenedioxyphenyl)-3-[(pivaloyloxy)methyl]-tetrahydrofuran
(2S,3R,4S)-4-(3',4'-Dimethoxybenzoyl)-2-(3",4"-methylenedioxyphenyl)-3-[(pivaloyloxy)methyl]-tetrahydrofuran
Title Journal or Book Year
Asymmetric syntheses of isostegane derivatives using trivalent iodine reagents Journal of the Chemical Society, Perkin Transactions 1 1996
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