(S(S),1R,2S)-(+)-DIMETHYL-1-(PARA-TOLUENESULFINYLAMINO)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-3-PHENYLETHYLPHOSPHONATE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | JpZ8PYpZWYs |
|---|---|
| InChI | InChI=1S/2C23H36NO5PSSi/c2*1-18-14-16-20(17-15-18)31(26)24-22(30(25,27-5)28-6)21(19-12-10-9-11-13-19)29-32(7,8)23(2,3)4/h2*9-17,21-22,24H,1-8H3/t2*21-,22-,31?/m11/s1 |
| InChIKey | IHENTAKIJSEMMQ-CFZSGYMMSA-N |
| Mol Weight | 995.3 g/mol |
| Molecular Formula | C46H72N2O10P2S2Si2 |
| Exact Mass | 994.364216 g/mol |
| Enantiomer InChIKey | IHENTAKIJSEMMQ-YGDQPIAKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(S(S),R)-(-)-O,O-DIETHYL-N-(PARA-TOLUENESULFINYL)-2-AMINO-2-PHENYL-PROPYL-PHOSPHONATE
(1R,2R)-2-[(Benzyloxycarbonyl)(methyl)amino]-1-[(tert-butyl)(dimethyl)silyloxy]-3-[(dimethyl)(1,1,2-trimethylpropyl)silyloxy]-1-phenylpropane
(1S,2R,sS)-Bis(diethylamino) .alpha.-(N-benzyl-2-aziridinyl)-.alpha.(N-tolylsulfonylamido)methanephosphoramide
(1R,2S,sS)-Bis(diethylamino) .alpha.-(N-benzyl-2-aziridinyl)-.alpha.(N-tolylsulfonylamido)methanephosphoramide
(4R)-4-tert-Butyldimethylsiloxy-4-phenyl-2S,3S-O-isopropylidenebutyl benzyl ether
(4S)-4-tert-Butyldimethylsiloxy-4-phenyl-2S,3S-O-isopropylidenebutyl benzyl ether
(1R,2S)-(-)-2-[(Dimethyl(2,2-dimethylethyl)silyloxy]-1,2-bis(3,4-dimethoxyphenyl)ethylamine
(1R,2S)-(-)-2-[(Dimethyl(2,2-dimethylethyl)silyloxy]-2-(3,4-dimethoxyphenyl)-1-(3,4,5-trimethoxyphenyl)ethylamine
(1S,2S)-3-tert-Butoxydiphenylsiloxy-1-tert-butyldimethylsiloxy-1-phenyl-2-trifluoroacetamidopropane
(2S,3S)-3-tert-Butyldiphenylsilyloxy-N,2-dimethyl-N-methoxy-4-phenylsulfonylbutanamide
| Title | Journal or Book | Year |
|---|---|---|
| Sulfinimine-Mediated Asymmetric Synthesis of β-Hydroxy α-Amino Phosphonates | The Journal of Organic Chemistry | 2003 |