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(S(S),1R,2S)-(+)-DIMETHYL-1-(PARA-TOLUENESULFINYLAMINO)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-3-METHYLBUTYLPHOSPHONATE

Compound with spectra: 2 NMR

(S(S),1R,2S)-(+)-DIMETHYL-1-(PARA-TOLUENESULFINYLAMINO)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-3-METHYLBUTYLPHOSPHONATE
SpectraBase Compound ID GGijq2FTO9J
InChI InChI=1S/C20H38NO5PSSi/c1-15(2)18(26-29(9,10)20(4,5)6)19(27(22,24-7)25-8)21-28(23)17-13-11-16(3)12-14-17/h11-15,18-19,21H,1-10H3/t18-,19+,28?/m1/s1
InChIKey VEOXXEBDJZSJBU-ZUDGUFDASA-N
Mol Weight 463.6 g/mol
Molecular Formula C20H38NO5PSSi
Exact Mass 463.197758 g/mol
Enantiomer InChIKey VEOXXEBDJZSJBU-NYCGYEKWSA-N

View Spectrum of (S(S),1R,2S)-(+)-DIMETHYL-1-(PARA-TOLUENESULFINYLAMINO)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-3-METHYLBUTYLPHOSPHONATE

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

View Spectrum of (S(S),1R,2S)-(+)-DIMETHYL-1-(PARA-TOLUENESULFINYLAMINO)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-3-METHYLBUTYLPHOSPHONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,2S,sS)-Dimethyl .alpha.-(N-benzyl-2-aziridinyl)-.alpha.(N-tolylsulfonylamido)methanephosphonate
(2R,sS)-Dimethyl .alpha.-(N-benzyl-2-aziridinyl)-.alpha.(N-tolylsulfonylamido)methanephosphonate
(S-(S),R)-(+)-O,O-DIETHYL-N-(PARA-TOLUENESULFINYL)-1-AMINO-4,4-DIMETHOXY-1-METHYLPENTYLPHOSPHONATE
(S(S),R)-(+)-O,O-DIETHYL-N-(PARA-TOLUENESULFINYL)-2-AMINO-2-PHENYLETHYL-PHOSPHONATE
(S(S),R)-(+)-O,O-DIMETHYL-N-(PARA-TOLUENESULFINYL)-2-AMINO-2-(PARA-TOLUENE)-ETHYLPHOSPHONATE
(S)-(1-R*,2-R*)-DIETHYL-[1-HYDROXY-2-(PARA-METHOXYPHENYL)-2-(PARA-TOLUENESULFONAMIDO)-ETHYL]-PHOSPHONATE
(3R,4R,5R)-6-TERT.-BUTYLDIMETHYLSILYLOXY-4-ETHYNYL-2-METHYL-5-[N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-AMINO]-HEXAN-3-OL
trans-4-[1-(4-Methoxyphenyl)ethenyl]-1-[(4-methylphenyl)sulfonyl]-3-pyrrolidinol
(3S,4S)-4-[1-(4-Methoxyphenyl)ethenyl]-1-[(4-methylphenyl)sulfonyl]-3-pyrrolidinol
Methyl 6.alpha.-[(tert-Butyldimethylsilyloxy)methyl]-4.beta.-(4'-methylbenzenesulfonyll)amino]cyclohexene-1-carboxylate
Title Journal or Book Year
Sulfinimine-Mediated Asymmetric Synthesis of β-Hydroxy α-Amino Phosphonates The Journal of Organic Chemistry 2003
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