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VESPERTILIN-ACETATE;3-BETA-ACETOXY-16-BETA-HYDROXY-DINORCHOL-5-ENIC-ACID-22->16-LACTONE
SpectraBase Compound ID FFLNXyTrOKS
InChI InChI=1S/C24H34O4/c1-13-21-20(28-22(13)26)12-19-17-6-5-15-11-16(27-14(2)25)7-9-23(15,3)18(17)8-10-24(19,21)4/h5,13,16-21H,6-12H2,1-4H3/t13-,16-,17+,18-,19-,20-,21-,23-,24-/m0/s1
InChIKey OWDSQNAIMXYQHD-TXWMIOKHSA-N
Mol Weight 386.5 g/mol
Molecular Formula C24H34O4
Exact Mass 386.24571 g/mol
Enantiomer InChIKey OWDSQNAIMXYQHD-BSNKDILASA-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
  • VESPERTILIN-ACETATE;3-BETA-ACETOXY-16-HYDROXY-DINORCHOL-5-ENIC-ACID-(22->16)-LACTONE
Title Journal or Book Year
Synthesis and plant growth promoting activity of dinorcholanic lactones bearing the 5α-hydroxy-6-oxo moiety The Journal of Steroid Biochemistry and Molecular Biology 2013
BF3·Et2O-induced stereoselective aldol reaction with benzaldehyde, and steroid sapogenins and its application to a convenient synthesis of dinorcholanic lactones Steroids 2012

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