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(5RS,6Z)-2,2,6-TRIMETHYL-8-(METHYLSULFONYL)-5-[(RS)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-OCT-6-EN-3-ONE

Compound with spectra: 1 NMR

(5RS,6Z)-2,2,6-TRIMETHYL-8-(METHYLSULFONYL)-5-[(RS)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-OCT-6-EN-3-ONE
SpectraBase Compound ID JM2gCKPGbZ9
InChI InChI=1S/C29H48O4S/c1-18(2)23-15-24(19(3)4)28(25(16-23)20(5)6)22(8)33-26(17-27(30)29(9,10)11)21(7)13-14-34(12,31)32/h13,15-16,18-20,22,26H,14,17H2,1-12H3/b21-13-/t22?,26-/m1/s1
InChIKey SVMLSYHDIFPWND-GUHAIMOLSA-N
Mol Weight 492.8 g/mol
Molecular Formula C29H48O4S
Exact Mass 492.327331 g/mol
Enantiomer InChIKey SVMLSYHDIFPWND-PJDCWEDZSA-N

View Spectrum of (5RS,6Z)-2,2,6-TRIMETHYL-8-(METHYLSULFONYL)-5-[(RS)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-OCT-6-EN-3-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(5SR,6Z)-2,2,6-TRIMETHYL-8-(METHYLSULFONYL)-5-[(RS)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-OCT-6-EN-3-ONE
(-)-(3R,4Z)-1-CYCLOPROPYL-4-METHYL-6-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEX-4-EN-1-ONE
(-)-(3S,4Z)-1-CYCLOPROPYL-4-METHYL-6-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEX-4-EN-1-ONE
(+/-)-(4RS,5Z,7SR)-5-METHYL-7-(METHYLSULFONYL)-4-[(RS)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-OCT-5-EN-2-ONE
(4S,5S)-5-But-3-enyl-4-[)R)-1-(2,4,6-triisopropylphenyl)ethoxy]pyrrolidin-2-one
(4R,5R)-5-ALLYL-4-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-PYRROLIDIN-2-ONE
1,1-BIS-(2,4,6-TRIISOPROPYLPHENYL)-3,3-DIMETHYL-1-BUTEN-1-OL
1-dimethylamino-2,2-bis[2,4,6-tri(propan-2-yl)phenyl]ethenol
Benzamide, N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-2,4,6-tris(1-methylethyl)-, (R*,R*)-
3-PHENYL-5-(2,4,6-TRIISOPROPYLPHENYL)-1,2,4-OXAZAPHOSPHOLE
Title Journal or Book Year
Development of a New Carbon−Carbon Bond Forming Reaction. New Organic Chemistry of Sulfur Dioxide. Asymmetric Four-Component Synthesis of Polyfunctional Sulfones The Journal of Organic Chemistry 2001
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