(+)-(E,S(S),2S,3R)-5-(N-METHYL-S-PHENYLSULFONIMIDOYL)-3-CYCLOHEXYL-2-(TOLUENE-4-SULFONYLAMINO)-PENT-4-ENOIC-ACID-ETHYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | GkVyehT3wjv |
|---|---|
| InChI | InChI=1S/C27H36N2O5S2/c1-4-34-27(30)26(29-36(32,33)24-17-15-21(2)16-18-24)25(22-11-7-5-8-12-22)19-20-35(31,28-3)23-13-9-6-10-14-23/h6,9-10,13-20,22,25-26,29H,4-5,7-8,11-12H2,1-3H3/b20-19+/t25-,26-,35?/m1/s1 |
| InChIKey | ZJVVUWKOPSHGNU-RJQQDBENSA-N |
| Mol Weight | 532.7 g/mol |
| Molecular Formula | C27H36N2O5S2 |
| Exact Mass | 532.206565 g/mol |
| Enantiomer InChIKey | ZJVVUWKOPSHGNU-FNEZEYTCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(+)-(E,S(S),2S,3S)-5-(N-METHYL-S-PHENYLSULFONIMIDOYL)-3-PHENYL-2-(2-METHYLPROPANE-2-SULFONYLAMINO)-PENT-4-ENOIC-ACID-ETHYLESTER
O(3),O(4)-ISOPROPYLIDENE-(2R,3S,4R)-(-)-3-HYDROXY-4-HYDROXYMETHYL-2-TOSYLAMINOBUTYROLACTONE
trans-6-(4-Chlorobutyl)-4-(phenylthio)-5-(tosylamino)-5,6-dihydropyran-2-one
Methyl 2-{N-[(benzyloxycarbonyl)methyl]-N-tosylamino}-4-oxo-4-phenylbutanoate
4-methyl-2-oxo-2H-chromen-7-yl (2S)-2-{[(4-methylphenyl)sulfonyl]amino}-3-phenylpropanoate
trans-6-(3-Chloropropyl)-4-(phenylthio)-5-(tosylamino)-5,6-dihydropyran-2-one
L-1-(p-TOLYLSULFONYL)PROLINE, 9-ANTHRYLMETHYL ESTER, HEMIETHANOLATE
1,5-ANHYDRO-3-O-BENZYL-2-DEOXY-2-N-TOLUENESULFON-6-O-TOLUENESULFONYL-D-MANNITOL
tert-Butyl[(diphenylmethylene)amino](2-{[(4-methylphenyl)sulfonyl]- amino}cyclohexyl) acetate
phenylalanine, N-[[2,3-dihydro-1-(1-oxopropyl)-1H-indol-5-yl]sulfonyl]-
| Title | Journal or Book | Year |
|---|---|---|
| Highly Selective Addition of Chiral, Sulfonimidoyl Substituted Bis(allyl)titanium Complexes to N-Sulfonyl α-Imino Esters: Asymmetric Synthesis of γ,δ-Unsaturated α-Amino Acids Bearing a Chiral, Electron-Withdrawing Nucleofuge at the δ-Position | Journal of the American Chemical Society | 2002 |