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(S)-1-[2'-(DIPHENYLPHOSPHINYL)-6'-PHENYLPHENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE

Compound with spectra: 2 NMR

(S)-1-[2'-(DIPHENYLPHOSPHINYL)-6'-PHENYLPHENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE
SpectraBase Compound ID 4topqcPXgdi
InChI InChI=1S/C29H28NO2P/c31-22-24-14-11-21-30(24)29-27(23-12-4-1-5-13-23)19-10-20-28(29)33(32,25-15-6-2-7-16-25)26-17-8-3-9-18-26/h1-10,12-13,15-20,24,31H,11,14,21-22H2/t24-/m0/s1
InChIKey DOPYDPXBRKXPPD-DEOSSOPVSA-N
Mol Weight 453.52 g/mol
Molecular Formula C29H28NO2P
Exact Mass 453.185766 g/mol
Enantiomer InChIKey DOPYDPXBRKXPPD-XMMPIXPASA-N
Racemate InChIKey DOPYDPXBRKXPPD-UHFFFAOYSA-N

View Spectrum of (S)-1-[2'-(DIPHENYLPHOSPHINYL)-6'-PHENYLPHENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE

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)-1-[2'-(DIPHENYLPHOSPHINYL)-6'-PHENYLPHENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
benzoic acid, 4-[[[5-bromo-1-(cyclopropylcarbonyl)-2,3-dihydro-1H-indol-7-yl]sulfonyl]amino]-, ethyl ester
2-Diphenylphosphoryl-1-isopropyl-indol-3-ol
1,3-Dimethyl-10-phenyl-5,10-dihydrophenophosphazine-10-oxide
[1,2,3,4,4a.beta.,5,6,8a.alpha.-Octahydronaphthyl-5-.beta.-(methoxy)methylene]tetracarbonyltriphenylphosphinetungsten
1H-indole-7-sulfonamide, 5-bromo-1-(cyclopropylcarbonyl)-2,3-dihydro-N-(3-methylphenyl)-
1-BROMOMETHYL-4-PHENYL-2-DIPHENYLPHOSPHINYL-NAPHTHALENE
4-BETA-CARBOXYMETHYL-(-)-EPICATECHIN_METHYLESTER
1,3,4,13b-tetrahydro-2H-pyrazino[1,2-f]phenanthridine, maleate(1:1)
1H-thieno[3,4-d]imidazol-2(3H)-one, tetrahydro-1-(4-methoxyphenyl)-3-(2-methylphenyl)-, 5,5-dioxide
N-(Prop-2-yn-1-yl)-2-diphenylphosphinoyl-3-hydroxyindole
Title Journal or Book Year
Development of Chiral (S)-Prolinol-Derived Ligands for Palladium-Catalyzed Asymmetric Allylic Alkylation:  Effect of a Siloxymethyl Group on the Pyrrolidine Backbone The Journal of Organic Chemistry 2004
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