(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-(DICYCLOHEXYLPHOSPHINITE)]
Compound with spectra: 1 NMR
![(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-(DICYCLOHEXYLPHOSPHINITE)]](/api/compound/7ZVjGFZK1Xq.png?ph=true&h=300&w=458 "(1S,2S)-1,2-BIS-[(TRITYLOXY)-METHYL]-ETHYLENE-BIS-(DICYCLOHEXYLPHOSPHINITE)]")
| SpectraBase Compound ID | 7ZVjGFZK1Xq |
|---|---|
| InChI | InChI=1S/C66H80O4P2/c1-11-31-53(32-12-1)65(54-33-13-2-14-34-54,55-35-15-3-16-36-55)67-51-63(69-71(59-43-23-7-24-44-59)60-45-25-8-26-46-60)64(70-72(61-47-27-9-28-48-61)62-49-29-10-30-50-62)52-68-66(56-37-17-4-18-38-56,57-39-19-5-20-40-57)58-41-21-6-22-42-58/h1-6,11-22,31-42,59-64H,7-10,23-30,43-52H2/t63-,64-/m0/s1 |
| InChIKey | LQHQYLXQLXLLBP-VKOZLBNWSA-N |
| Mol Weight | 999.3 g/mol |
| Molecular Formula | C66H80O4P2 |
| Exact Mass | 998.553185 g/mol |
| Enantiomer InChIKey | LQHQYLXQLXLLBP-CEOZETRISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5-O-ALLYL-2,3,4-TRI-O-BENZYL-1-O-TRITYL-D-RIBITOL
2,3,4-Trimethoxy-5,5-bis(ethylthio)pentyl Trityl Ether
6-O-Triphenylmethyl-d-glucopyranose
(2R,4R,5R)-5-Ethyl-2-methyl-4-(trityloxymethyl)-1,3-dioxan-5-ol
(2R,4S,5R)-5-Ethyl-2-methyl-4-(trityloxymethyl)-1,3-dioxan-5-ol
METHYL-2-DEOXY-3-O-METHYL-6-O-TRIPHENYLMETHYL-ALPHA-D-ARABINO-HEXAPYRANOSIDE
(+/-)-2,3,4,5-TETRA-O-METHYL-6-O-TRITYLGALACTOSE
2,3,4,5-TETRA-O-METHYL-6-O-TRITYL-L-GULOSE
OCTYL-5-O-TRITYL-ALPHA-D-ARABINOFURANOSIDE
(2S,4S,6R)-2-(2,2-DIMETHYL-1-HYDROXYPROPYL)-4-TRITYLOXYMETHYLBUTANOLIDE
| 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 |