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(-)-(4R,5Z)-5-METHYL-7-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEPT-5-EN-2-ONE

Compound with spectra: 2 NMR

(-)-(4R,5Z)-5-METHYL-7-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEPT-5-EN-2-ONE
SpectraBase Compound ID 9i4qAXPOJej
InChI InChI=1S/C26H42O4S/c1-16(2)22-14-23(17(3)4)26(24(15-22)18(5)6)21(9)30-25(13-20(8)27)19(7)11-12-31(10,28)29/h11,14-18,21,25H,12-13H2,1-10H3/b19-11-/t21-,25-/m0/s1
InChIKey NESCFTJRCJFAEC-NPYWNRMPSA-N
Mol Weight 450.7 g/mol
Molecular Formula C26H42O4S
Exact Mass 450.280381 g/mol
Enantiomer InChIKey NESCFTJRCJFAEC-BHBNTXBJSA-N

View Spectrum of (-)-(4R,5Z)-5-METHYL-7-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEPT-5-EN-2-ONE

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

View Spectrum of (-)-(4R,5Z)-5-METHYL-7-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEPT-5-EN-2-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (-)-(4S,5Z)-5-METHYL-7-(METHYLSULFONYL)-3-[(S)-1-(2,4,6-TRIISOPROPYLPHENYL)-ETHOXY]-HEPT-5-EN-2-ONE
(3R,4Z)-4-METHYL-6-(METHYLSULFONYL)-3-[(R)-1-(2-NAPHTHYL)-ETHOXY]-1-PHENYLHEX-4-EN-1-ONE
(3S,4Z)-4-METHYL-6-(METHYLSULFONYL)-3-[(R)-1-(2-NAPHTHYL)-ETHOXY]-1-PHENYLHEX-4-EN-1-ONE
methyl (2S)-4-methyl-2-{[(2,4,6-triisopropylphenyl)sulfonyl]amino}pentanoate
3-(2,4,6-triisopropylbenzoyl)benzoic acid
Propanoic acid, 2,2-dimethyl-, 2,2-dimethyl-1-[2,4,6-tris(2,2-dimethylpropyl)phenyl]propyl ester
Benzeneethanol, 4-[(acetyloxy)methyl]-3-[3-(acetyloxy)-2-methyl-1-propenyl]-2,6-dimethyl-, acetate, (E)-
[1,1'-Biphenyl]ol, ar-methyl-2',4',6'-tris(1-methylethyl)-
cis-3,3a,4,5-Tetrahydro-7-(2,4,6-trimethylphenyl)-7H-pyrano[3,4-c]isoxazole
alpha-methyl-6-tert-butyl-1,1-dimethyl-4-indanemethanol
N-1-(1-Ethyl-2-oxopentyl)-2,4,6-triisopropyl-1-benzenesulfonamide
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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