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(1S,2S)-1,2-[BIS-(3,5-TRIFLUOROMETHYLPHENYL)-PHOSPHINOXY]-CYCLOHEXANE

Compound with spectra: 3 NMR

(1S,2S)-1,2-[BIS-(3,5-TRIFLUOROMETHYLPHENYL)-PHOSPHINOXY]-CYCLOHEXANE
SpectraBase Compound ID FWrhhT8oIk7
InChI InChI=1S/C38H22F24O2P2/c39-31(40,41)17-5-18(32(42,43)44)10-25(9-17)65(26-11-19(33(45,46)47)6-20(12-26)34(48,49)50)63-29-3-1-2-4-30(29)64-66(27-13-21(35(51,52)53)7-22(14-27)36(54,55)56)28-15-23(37(57,58)59)8-24(16-28)38(60,61)62/h5-16,29-30H,1-4H2/t29-,30-/m1/s1
InChIKey XKSHCNIWRGZUGN-LOYHVIPDSA-N
Mol Weight 1028.5 g/mol
Molecular Formula C38H22F24O2P2
Exact Mass 1028.07118 g/mol
Enantiomer InChIKey XKSHCNIWRGZUGN-KYJUHHDHSA-N

View Spectrum of (1S,2S)-1,2-[BIS-(3,5-TRIFLUOROMETHYLPHENYL)-PHOSPHINOXY]-CYCLOHEXANE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of (1S,2S)-1,2-[BIS-(3,5-TRIFLUOROMETHYLPHENYL)-PHOSPHINOXY]-CYCLOHEXANE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent THF-D8

View Spectrum of (1S,2S)-1,2-[BIS-(3,5-TRIFLUOROMETHYLPHENYL)-PHOSPHINOXY]-CYCLOHEXANE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1R,2R)-1,2-CYCLOHEXYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]
2,2,2-TRIPHENYL-4,5-TETRAMETHYLENE-1,3,2-DIOXAPHOSPHOLANE
8,8,8-tri(phenyl)-7,9-dioxa-8$l^{5}-phosphabicyclo[4.3.0]nonane
PHCRVFHQYFXFGG-DNQXCXABSA-N
DIETHYL-(2R,3R)-2,3-BIS-[[DI-(4-FLUOROPHENYL)-PHENYLPHOSPHINO]-OXY]-SUCCINATE
N-(alpha,alpha,alpha,alpha',alpha',alpha'-hexafluoro-3,5-xylyl)-2-methylsuccinimide
L-733,060
L-733 060 HCl
NEOPENTYLOXY-(PHENACYL)-DIPHENYLOXYPHOSPHONIUM-BROMIDE
2-METHOXY-2,2-DIPHENYL-4,4,5,5-TETRAMETHYL-1,3,2-DIOXAPHOSPHOLAN
4-(alpha,alpha,alpha,alpha',alpha',alpha'-HEXAFLUORO-3,5-XYLYL)-3-THIO-1-(3,4,5-TRIMETHOXYHYDROCINNAMOYL)SEMICARBAZIDE
Title Journal or Book Year
Substituent Effects of Ligands on Asymmetric Induction in a Prototypical Palladium-Catalyzed Allylation Reaction:  Making Both Enantiomers of a Product in High Optical Purity Using the Same Source of Chirality The Journal of Organic Chemistry 1999
Electronic Effects in Asymmetric Catalysis:  Structural Studies of Precatalysts and Intermediates in Rh-Catalyzed Hydrogenation of Dimethyl Itaconate and Acetamidocinnamic Acid Derivatives Using C2-Symmetric Diarylphosphinite Ligands The Journal of Organic Chemistry 1999
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