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#1;(+/-)-LINDEROL-A;RAC-(5AR,6R,9R,9AS)-4-CINNAMOYL-3,6-DIHYDROXY-1-METHOXY-6-METHYL-9-(1-METHYLETHYL)-5A,6,7,8,9,9A-HEXAHYDRODIBENZOFURAN;SYNTHETIC-PRODUCT
SpectraBase Compound ID DywDfygREPQ
InChI InChI=1S/C26H30O5/c1-15(2)17-12-13-26(3,29)25-21(17)23-20(30-4)14-19(28)22(24(23)31-25)18(27)11-10-16-8-6-5-7-9-16/h5-11,14-15,17,21,25,28-29H,12-13H2,1-4H3/b11-10+/t17-,21+,25-,26-/m0/s1
InChIKey QNFHIVKGSJTPDD-GXNIJBQLSA-N
Mol Weight 422.52 g/mol
Molecular Formula C26H30O5
Exact Mass 422.209324 g/mol
Enantiomer InChIKey QNFHIVKGSJTPDD-XUUFYWMYSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • #1;(+/-)-LINDEROL-A;RAC-(5AR,6R,9R,9AS)-4-CINNAMOYL-3,6-DIHYDROXY-1-METHOXY-6-METHYL-9-(1-METHYLETHYL)-5A,6,7,8,9,9A-HEXAHYDRODIBENZOFURAN;NATURAL-PRODUCT
Title Journal or Book Year
First Total Synthesis of (±)-Linderol A, a Tricyclic Hexahydrodibenzofuran Constituent of Lindera umbellata Bark, with Potent Inhibitory Activity on Melanin Biosynthesis of Cultured B-16 Melanoma Cells The Journal of Organic Chemistry 2003
Unknown Identification

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