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(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]

Compound with spectra: 1 NMR

(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]
SpectraBase Compound ID 8mS4462RMZQ
InChI InChI=1S/C74H48F24O4P2/c75-67(76,77)51-31-52(68(78,79)80)36-59(35-51)103(60-37-53(69(81,82)83)32-54(38-60)70(84,85)86)101-63(43-99-65(45-19-7-1-8-20-45,46-21-9-2-10-22-46)47-23-11-3-12-24-47)64(44-100-66(48-25-13-4-14-26-48,49-27-15-5-16-28-49)50-29-17-6-18-30-50)102-104(61-39-55(71(87,88)89)33-56(40-61)72(90,91)92)62-41-57(73(93,94)95)34-58(42-62)74(96,97)98/h1-42,63-64H,43-44H2/t63-,64-/m0/s1
InChIKey GWWQEXIADDKGOT-VKOZLBNWSA-N
Mol Weight 1519.1 g/mol
Molecular Formula C74H48F24O4P2
Exact Mass 1518.26446 g/mol
Enantiomer InChIKey GWWQEXIADDKGOT-CEOZETRISA-N

View Spectrum of (1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
AAQGKPSOBOBUGS-OJDZSJEKSA-N
METHYL-2,3-DI-O-METHYL-6-O-TRIPHENYLMETHYL-ALPHA-D-GALACTOPYRANOSIDE
D-Ribonic acid, 5-O-(triphenylmethyl)-, .gamma.-lactone, 2,3-diacetate
2,3-O-ISOPROPYLIDENE-5-O-TRITYL-ALPHA-D-RIBOFURANOSIDE
4-METHOXYCINNAMYL-6-TRITYL-O-BETA-D-GLUCOPYRANOSIDE
5'-O-(4,4'-DIMETHOXYTRITYL)-1'-DEOXY-1'-PHENYL-BETA-D-RIBOFURANOSE
10;2',3'-BIS-O-(TRIPHENYLMETHYL)-2',3'-SECOURIDINE;1-[(1R)-1-[(1S)-2-HYDROXY-1-[(TRIPHENYLMETHOXY)-METHYL]-ETHOXY]-2-(TRIPHENYLMETHOXY)-ETHYL]-PYRIMIDINE-2,4-(
(2R*,3S*)-3-DIPHENYLPHOSPHINOYL-2-METHYL-3-TRIMETHYLSILYL-1-TRIPHENYLMETHOXYPROPANE
2',3'-DI-O-ACETYL-5'-O-(TRIPHENYLMETHYL)-2',3'-SECOURIDINE;1-[(1R)-2-ACETOXY-1-((1R)-2-ACETOXY-1-[(TRIPHENYLMETHOXY)-METHYL]-ETHOXY)-ETHYL]-URACIL
2,3,5-TRI-O-BENZYL-4-O-METHANESULFONYL-1-O-TRITYL-D-ARABINITOL
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
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