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(1''R*,2''E,2'R*,3'S*,4'S*)-7-[2'-(TERT.-BUTYLSULFINYLMETHYL)-2'-HYDROXY-4'-(1''-PHENYLTHIO-OCT-2''-ENYL)-TETRAHYDROFURAN-3'-YL]-HEPT-5-YNOIC-ACID

Compound with spectra: 1 NMR

(1''R*,2''E,2'R*,3'S*,4'S*)-7-[2'-(TERT.-BUTYLSULFINYLMETHYL)-2'-HYDROXY-4'-(1''-PHENYLTHIO-OCT-2''-ENYL)-TETRAHYDROFURAN-3'-YL]-HEPT-5-YNOIC-ACID
SpectraBase Compound ID IHLbBxWjkZR
InChI InChI=1S/C30H44O6S2/c1-5-6-7-8-15-20-27(37-24-17-12-11-13-18-24)25-22-36-30(33,23-38(34,35)29(2,3)4)26(25)19-14-9-10-16-21-28(31)32/h11-13,15,17-18,20,25-27,33H,5-8,10,16,19,21-23H2,1-4H3,(H,31,32)/b20-15+/t25-,26+,27-,30-/m0/s1
InChIKey MMVIMWPNRATHRX-PZHHWPKRSA-N
Mol Weight 564.8 g/mol
Molecular Formula C30H44O6S2
Exact Mass 564.257931 g/mol
Enantiomer InChIKey MMVIMWPNRATHRX-SOJKYUODSA-N

View Spectrum of (1''R*,2''E,2'R*,3'S*,4'S*)-7-[2'-(TERT.-BUTYLSULFINYLMETHYL)-2'-HYDROXY-4'-(1''-PHENYLTHIO-OCT-2''-ENYL)-TETRAHYDROFURAN-3'-YL]-HEPT-5-YNOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1''R*,2''E,2'S*,3'R*,4'R*)-7-[2'-(TERT.-BUTYLSULFINYLMETHYL)-2'-HYDROXY-4'-(1''-PHENYLTHIO-OCT-2''-ENYL)-TETRAHYDROFURAN-3'-YL]-HEPT-5-YNOIC-ACID
METHYL-7-[2'-(TERT.-BUTYLSULFINYLMETHYL)-2'-HYDROXY-4'-(1''-PHENYLTHIO-OCT-2''-ENYL)-TETRAHYDROFURAN-3'-YL]-HEPT-5-YNOATE;(DIASTEREOMER-A)
(3RS,4SR,3'SR)-4'-Methyl-3'-(phenylthio)(1-azabicyclo[2.2.2]octan-3-spiro-2'-tdihydrofuran-5'-one)
exo,exo-2,3-Dibromo-exo-5-endo-6-bis(phenylsulfonyl)-7-oxabicyclo[2.2.1]heptane
(1R,4S,7R,8R,11S)-7-[4-(Ethoxycarbonyl)-2-methylbut-2-yl]-2,10-dioxatricyclo[6.2.1.0(4,11)]undec-5-en-9-one isomer
CYCLCZHEURCWBE-JLOCXQCDSA-N
3-[(3-phenyl-1,8-naphthyridin-2-yl)hydrazo]-2-indolone
Tricyclo[7.2.2.0(3,8)]trideca-5,12-dien-2-one, 1-methoxy-4-methyl-
PHENYL-6-DEOXY-3,4-O-ISOPROPYLIDENE-2-O-PIVALOYL-1-THIO-BETA-D-GALACTOSIDE
8-Methoxy-2,4-bis(methylsulfanyl)-5,6-dihydrobenzo[f]isoquinoline
Title Journal or Book Year
The Preparation of 9-Oxo-10-Oxaprostanoids by the Conjugate Addition of (E)-1-(Phenylthio)Oct-2-Enyllithium to γ-Crotonolactone and the Direct Alkylation of the Derived Enolate With Methyl 7-Bromohept-5-ynoate and Related Electrophiles Australian Journal of Chemistry 1987
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