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METHYL-(E)-9,15-DIHYDROXY-11-TERT.-BUTOXY-PROST-13-EN-5-YNOATE;(15-DIASTEREOMER-A)

Compound with spectra: 2 NMR

METHYL-(E)-9,15-DIHYDROXY-11-TERT.-BUTOXY-PROST-13-EN-5-YNOATE;(15-DIASTEREOMER-A)
SpectraBase Compound ID Cu4fcAUQLzX
InChI InChI=1S/C25H42O5/c1-6-7-10-13-19(26)16-17-21-20(14-11-8-9-12-15-24(28)29-5)22(27)18-23(21)30-25(2,3)4/h16-17,19-23,26-27H,6-7,9-10,12-15,18H2,1-5H3/b17-16+
InChIKey XWYVUZKQXFVDLJ-WUKNDPDISA-N
Mol Weight 422.6 g/mol
Molecular Formula C25H42O5
Exact Mass 422.303224 g/mol

View Spectrum of METHYL-(E)-9,15-DIHYDROXY-11-TERT.-BUTOXY-PROST-13-EN-5-YNOATE;(15-DIASTEREOMER-A)

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

View Spectrum of METHYL-(E)-9,15-DIHYDROXY-11-TERT.-BUTOXY-PROST-13-EN-5-YNOATE;(15-DIASTEREOMER-A)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • METHYL-(E)-9,15-DIHYDROXY-11-TERT.-BUTOXY-PROST-13-EN-5-YNOATE;(15-DIASTEREOMER-B)
Methyl (E)-9,15-Dihydroxy-11-t-butoxypropst-13-en-5-ynoate
PGF(2-ALPHA)-9-O-ACETATE-METHYLESTER;9-ALPHA-ACETYLOXY-11-ALPHA,15S-DIHYDROXY-PROSTA-5Z,13E-DIENOIC-ACID-METHYLESTER
9-O-Acetoxy-17,18-didehydro-PGF(3.alpha.) methyl ester
9-O-Acetoxy-PGF(3.alpha.) methyl ester
(Z)-7-[(1R,2S,3S,5R)-5-acetoxy-3-hydroxy-2-[(E)-3-ketooct-1-enyl]cyclopentyl]hept-5-enoic acid ethyl ester
10,10-DIMETHYL-PGF-1-ALPHA
10,10-DIMETHYL-11-EPI-PGF-1-BETA
10,10-DIMETHYL-PGF-1-BETA
3-Oxacarbacyclin
7-{3,5-DIHYDROXY-2-{2-[2-(PHENOXYMETHYL)-1,3-DIOXOLAN-2-YL]VINYL}CYCLOPENTYL}-5-HEPTENOIC ACID, COMPOUND WITH 2-AMINO-2-(HYDROXYMETHYL)-1,3-PROPANEDIOL (1:1)
Title Journal or Book Year
An Extremely Simple Route to a Prostaglandin Precursor: Hexamethylphosphoric-Triamide-Mediated Conjugate Addition of 1-(Phenylthio)Oct-2-Enyllithium to 4-Tert-Butoxycyclopent-2-Enone and Triphenyltin-Chloride-Assisted Reaction of the Enolate With Methyl 7-Iodohept-5-Ynoate Australian Journal of Chemistry 1987

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