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TRANS-2-(4-HYDROXY-3,5-DIMETHOXYBENZYL)-3-(ALPHA-HYDROXY-3,4-METHYLENEDIOXYBENZYL)-BUTANOLIDE;EPIMER-#1
SpectraBase Compound ID 5gm9xFlGY8d
InChI InChI=1S/C21H22O8/c1-25-17-6-11(7-18(26-2)20(17)23)5-13-14(9-27-21(13)24)19(22)12-3-4-15-16(8-12)29-10-28-15/h3-4,6-8,13-14,19,22-23H,5,9-10H2,1-2H3/t13-,14+,19?/m1/s1
InChIKey GKLCKTAHWKLKNQ-YCENCERGSA-N
Mol Weight 402.4 g/mol
Molecular Formula C21H22O8
Exact Mass 402.131468 g/mol
Enantiomer InChIKey GKLCKTAHWKLKNQ-PFCANICASA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum H1-43-2455-19
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum H1-43-2455-19
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • TRANS-2-(4-HYDROXY-3,5-DIMETHOXYBENZYL)-3-(ALPHA-HYDROXY-3,4-METHYLENEDIOXYBENZYL)-BUTANOLIDE;EPIMER-#2
  • (3R,4R)-4-[1,3-benzodioxol-5-yl(hydroxy)methyl]-3-(4-hydroxy-3,5-dimethoxy-benzyl)tetrahydrofuran-2-one
Title Journal or Book Year
Studies with Plant Cell Cultures of Cassia didymobotrya. VII. Enzyme Catalyzed Biotransformation of Dibenzylbutanolides to Podophyllotoxin Analogues and Related Compounds HETEROCYCLES 1996

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