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DIETHYL-[S-(S),1S,2R]-(+)-1-(PARA-TOLUENESULFONYLOXY)-2-PHENYL-2-(PARA-TOLUENESULFINAMIDE)-ETHYLPHOSPHONATE

Compound with spectra: 2 NMR

DIETHYL-[S-(S),1S,2R]-(+)-1-(PARA-TOLUENESULFONYLOXY)-2-PHENYL-2-(PARA-TOLUENESULFINAMIDE)-ETHYLPHOSPHONATE
SpectraBase Compound ID 6sLgSDU6XUt
InChI InChI=1S/C26H32NO7PS2/c1-5-32-35(28,33-6-2)26(34-37(30,31)24-18-14-21(4)15-19-24)25(22-10-8-7-9-11-22)27-36(29)23-16-12-20(3)13-17-23/h7-19,25-27H,5-6H2,1-4H3/t25-,26-,36?/m1/s1
InChIKey GIHLYATUVBFLRZ-VQABWYAYSA-N
Mol Weight 565.6 g/mol
Molecular Formula C26H32NO7PS2
Exact Mass 565.135782 g/mol
Enantiomer InChIKey GIHLYATUVBFLRZ-XDUWZGRSSA-N

View Spectrum of DIETHYL-[S-(S),1S,2R]-(+)-1-(PARA-TOLUENESULFONYLOXY)-2-PHENYL-2-(PARA-TOLUENESULFINAMIDE)-ETHYLPHOSPHONATE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of DIETHYL-[S-(S),1S,2R]-(+)-1-(PARA-TOLUENESULFONYLOXY)-2-PHENYL-2-(PARA-TOLUENESULFINAMIDE)-ETHYLPHOSPHONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[2R,6R,2(4S,5S)]-2-(4-methyl-2-thioxo-1,3-dioxolanyl)-6-methyl-N-(p-tolylsulfonyl)piperidine
(1S,2R,4S,1'R,2'R)-N-[trans-2'-[7,7-Dimethyl-2-hydrxybicyclo[2.2.1]hept-1-ylmethylsulfonamino]cyclohexyl]-4'-methylbenzenesulfonamide
5-exo-Bromo-2-(4'-methoxy-benzyl)-6-endo-phenylselenenyl-2-aza-bicyclo(2.2.1)heptan-3-one
2-ACETYLAMINO-5-TRIFLUOROMETHYL-7-(2-FURYL)-1,8-NAPHTHYRIDINE
HWZONAPYAIGQQZ-PFOAOIIYSA-N
ZMWDUEBZKDHPKB-UHFFFAOYSA-J
2,4-BIS(TRIFLUOROMETHYL)-7-{4-[(p-CHLOROPHENYL)SULFONYL]-1-PIPERAZINYL}-1,8-NAPHTHYRIDINE
(3R,5R)-5-butyl-1,2-bis(p-toluenesulfonyl)pyrazolidin-3-ol
7-(2-ALLYLOXY-1-PHENYLETHYL)-2-AMINOPURIN-6-ONE
1-[2-(1-PHENYLSULFONYLPYRROLO-[2.3-B]-PYRIDIN-3-YL)-ETHYL]-4-PIPERIDONE
Title Journal or Book Year
Asymmetric Synthesis of Aziridine 2-Phosphonates from Enantiopure Sulfinimines (N-Sulfinyl Imines). Synthesis of α-Amino Phosphonates The Journal of Organic Chemistry 2003
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