(1S,2S)-1,2-BIS-[(BENZYLOXY)-METHYL]-ETHYLENE-BIS-(DICYCLOHEXYLPHOSPHINITE)]
Compound with spectra: 1 NMR
![(1S,2S)-1,2-BIS-[(BENZYLOXY)-METHYL]-ETHYLENE-BIS-(DICYCLOHEXYLPHOSPHINITE)]](/api/compound/Jhu7P5yCYHn.png?ph=true&h=300&w=458 "(1S,2S)-1,2-BIS-[(BENZYLOXY)-METHYL]-ETHYLENE-BIS-(DICYCLOHEXYLPHOSPHINITE)]")
| SpectraBase Compound ID | Jhu7P5yCYHn |
|---|---|
| InChI | InChI=1S/C42H64O4P2/c1-7-19-35(20-8-1)31-43-33-41(45-47(37-23-11-3-12-24-37)38-25-13-4-14-26-38)42(34-44-32-36-21-9-2-10-22-36)46-48(39-27-15-5-16-28-39)40-29-17-6-18-30-40/h1-2,7-10,19-22,37-42H,3-6,11-18,23-34H2/t41-,42-/m0/s1 |
| InChIKey | QMKUZNYUAIEZEJ-COCZKOEFSA-N |
| Mol Weight | 694.9 g/mol |
| Molecular Formula | C42H64O4P2 |
| Exact Mass | 694.427985 g/mol |
| Enantiomer InChIKey | QMKUZNYUAIEZEJ-NCRNUEESSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(Z)-3-[(4S,5S)-4,5-bis(benzoxymethyl)-1,3-dioxolan-2-yl]-2-bromo-acrylic acid ethyl ester
(2R,3R)-1-Benzyloxy-2,4-isopropylidenedioxy-3-(4-methoxybenzyloxy)butane
(4S,5R)-(5-Benzyloxymethyl-2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-(2,2-dimethoxyethyl)amine
Benzyl [5'-(Benzyloxymethyl)-2',2'-dimethyl-1',3'-dioxolan-4'-yl]methyl] Amine
2,4-DI-O-BENZYL-L-ERYTHRITOL-1,3-O-CYCLIC-SULFATE
METHYL-4,6-DI-O-BENZYL-2,3-DIDEOXY-ALPHA-D-THREO-HEXOSIDE
METHYL-4,6-DI-O-BENZYL-2,3-DIDEOXY-BETA-D-THREO-HEXOSIDE
1-[(4R,5R)-2,2-dimethyl-5-(phenylmethoxymethyl)-1,3-dioxolan-4-yl]ethanone
1,4-ANHYDRO-2,3,5-TRI-O-BENZYL-D-ARABINITOL
Acetamide, N-[2-(acetyloxy)-1-[(acetyloxy)methyl]-3-(phenylmethoxy)propyl]-, (R*,R*)-(.+-.)-
| 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 |