(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-[4-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]
Compound with spectra: 1 NMR
![(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-[4-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]](/api/compound/JlN6Cejdvwd.png?ph=true&h=300&w=458 "(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-[4-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]")
| SpectraBase Compound ID | JlN6Cejdvwd |
|---|---|
| InChI | InChI=1S/C70H52F12O4P2/c71-67(72,73)55-31-39-59(40-32-55)87(60-41-33-56(34-42-60)68(74,75)76)85-63(47-83-65(49-19-7-1-8-20-49,50-21-9-2-10-22-50)51-23-11-3-12-24-51)64(48-84-66(52-25-13-4-14-26-52,53-27-15-5-16-28-53)54-29-17-6-18-30-54)86-88(61-43-35-57(36-44-61)69(77,78)79)62-45-37-58(38-46-62)70(80,81)82/h1-46,63-64H,47-48H2/t63-,64-/m0/s1 |
| InChIKey | BIKBDBDNNWMWCD-VKOZLBNWSA-N |
| Mol Weight | 1247.1 g/mol |
| Molecular Formula | C70H52F12O4P2 |
| Exact Mass | 1246.314922 g/mol |
| Enantiomer InChIKey | BIKBDBDNNWMWCD-CEOZETRISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-4-O-METHANESULFONYL-6-O-TRIPHENYLMETHYL-2,3-DIDEOXY-D-ERYTHRO-HEXOPYRANOSIDE
(1S,2S)-1,2-BIS-[(BENZYLOXY)-METHYL]-ETHYLENE-BIS-[3,5-BIS-(TRIFLUOROMETHYL)-PHENYLPHOSPHINITE]
6-O-(TERT.-BUTYLDIMETHYLSILYL)-2,3,4,5-TETRA-O-METHYL-1-O-TRITYL-D-GLUCITOL
1-O-(TERT.-BUTYLDIMETHYLSILYL)-2,3,4,5-TETRA-O-METHYL-6-O-TRITYL-D-GLUCITOL
1-O-(TERT.-BUTYLDIMETHYLSILYL)-2,3,4,5-TETRA-O-METHYL-6-O-TRITYL-D-GALACITOL
6-O-(TERT.-BUTYLDIMETHYLSILYL)-2,3,4-TRI-O-METHYL-1-O-TRITYL-D-GLUCITOL
1-O-(TERT.-BUTYLDIMETHYLSILYL)-3,4,5-TRI-O-METHYL-6-O-TRITYL-L-GALACITOL
(2R,3S,4S)-2,3,4-TRIS-(BENZYLOXY)-5-(TRITYLOXY)-PENTANAL
(2R,3S,4R)-2,3,4-TRIS-(BENZYLOXY)-5-(TRITYLOXY)-PENTANAL
4-AMIDO-2,3,5-TRI-O-BENZYL-4-DEOXY-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 |