(1S,2S)-1,2-DIPHENYLETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]
Compound with spectra: 1 NMR
![(1S,2S)-1,2-DIPHENYLETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]](/api/compound/3EsAq7W8mY9.png?ph=true&h=300&w=458 "(1S,2S)-1,2-DIPHENYLETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]")
| SpectraBase Compound ID | 3EsAq7W8mY9 |
|---|---|
| InChI | InChI=1S/C46H24F24O2P2/c47-39(48,49)25-11-26(40(50,51)52)16-33(15-25)73(34-17-27(41(53,54)55)12-28(18-34)42(56,57)58)71-37(23-7-3-1-4-8-23)38(24-9-5-2-6-10-24)72-74(35-19-29(43(59,60)61)13-30(20-35)44(62,63)64)36-21-31(45(65,66)67)14-32(22-36)46(68,69)70/h1-22,37-38H/t37-,38-/m0/s1 |
| InChIKey | PREKGODFKSAYSS-UWXQCODUSA-N |
| Mol Weight | 1126.6 g/mol |
| Molecular Formula | C46H24F24O2P2 |
| Exact Mass | 1126.08683 g/mol |
| Enantiomer InChIKey | PREKGODFKSAYSS-XPSQVAKYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
DIETHYL-(2R,3R)-2,3-BIS-[[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINO]-OXY]-SUCCINATE
(1S,2S)-1-PHENYL-2-(N-METHYL-N-DIPHENYLPHOSPHINOAMINO)-1-(DIPHENYLPHOSPHINOXY)PROPANE
DIETHYL-(2R,3R)-2,3-BIS-[[3,5-BIS-(TRIMETHYLSILYL)-PHENYLPHOSPHINO]-OXY]-SUCCINATE
O-(ALPHA-DIPHENYLPHOSPHINOBENZYL)DIPHENYLPHOSPHINATE
3,4-BIS-O-(DIPHENYLPHOSPHINO)-1,6-DI-O-(TRIISOPROPYLSILYL)-2,5-ANHYDRO-D-MANNITOL
2-[(4S,5S)-2-(3-cyclopropylidenepropyl)-4,5-diphenyl-1,3-dioxolan-2-yl]ethynyl-trimethyl-silane
2,5,6-Triphenyl-5,6-dihydro-4H-1,3-oxazine
2,2,2,5-TETRAPHENYL-1,3,4,2(LAMBDA-5)-OXADIAZAPHOSPHOLINE
N-[3,5-bis(trifluoromethyl)phenyl]-3-[(4-nitro-1H-pyrazol-1-yl)methyl]benzamide
2,2,2,2',2',2'-hexaphenyl-5,5'-bis[1,2.lambda.(5)-oxaphospholane]
| 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 |