1,2-BIS-[(2-S,3-S,4-S,5-S)-3,4-BIS-(TERT.-BUTYLOXY)-2,5-DIMETHYLPHOSPHOLANYL]-ETHANE_BH3_ADDUCT
Compound with spectra: 1 NMR
![1,2-BIS-[(2-S,3-S,4-S,5-S)-3,4-BIS-(TERT.-BUTYLOXY)-2,5-DIMETHYLPHOSPHOLANYL]-ETHANE_BH3_ADDUCT](/api/compound/7qE7Z6h8vAV.png?ph=true&h=300&w=458 "1,2-BIS-[(2-S,3-S,4-S,5-S)-3,4-BIS-(TERT.-BUTYLOXY)-2,5-DIMETHYLPHOSPHOLANYL]-ETHANE_BH3_ADDUCT")
| SpectraBase Compound ID | 7qE7Z6h8vAV |
|---|---|
| InChI | InChI=1S/C30H66B2O4P2/c1-19-23(33-27(5,6)7)24(34-28(8,9)10)20(2)37(19,31)17-18-38(32)21(3)25(35-29(11,12)13)26(22(38)4)36-30(14,15)16/h19-26,37-38H,17-18,31-32H2,1-16H3/t19-,20-,21-,22-,23+,24+,25+,26+/m0/s1 |
| InChIKey | KVJMZGLJRMWKRG-HITYTLSWSA-N |
| Mol Weight | 574.4 g/mol |
| Molecular Formula | C30H66B2O4P2 |
| Exact Mass | 574.462245 g/mol |
| Enantiomer InChIKey | KVJMZGLJRMWKRG-DWFOAMBESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
[[(4S,5S)-2,2-DIMETHYL-1,3-DIOXOLANE-4,5-DIYL]-DI-(R)-ETHYLIDENE]-BIS-[DI-(4-METHOXYPHENYL)-PHOSPHINE]
D-MANNO-(E)-TETRADEC-6-EN-1,2,3,4,5-PENTOL, 1,2:4,5-DI-O-ISOPROPYLIDENE-
3-(Hydroxy)-1,2:4,5-Bis(diisopropylidenedioxy)dodec-6-ene
(Z,1R)-1-[(4R,5R)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-1,3-dioxolan-4-yl]-3-hexen-1-ol
BYSRCBPAUDRGLY-PIEMUWSUSA-N
1-O-Benzyl-3,4:5,6-di-O-isopropylidene-D-glucitol
DIETHYL-[2-HYDROXY-2-(1-METHYL-2-PROPENYL)-CYCLOHEXYL]-PHOSPHONATE;MAJOR-DIASTEREOMER
(1R)-1-[(4R,5R)-5-[(4R,5R)-2,2-dimethyl-5-methylol-1,3-dioxolan-4-yl]-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol
N-iso-Propyl-2-(2,3-methylenedioxyphenyl)butan-1-amine AC
1-C-(CYCLOPENTA-2,4-DIENYLIDENE)-1-DEOXY-2,3:4,5-DI-O-ISOPROPYLIDENE-D-ARABINITOL
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of a New Class of Functionalized Chiral Bisphospholane Ligands and the Application in Enantioselective Hydrogenations | The Journal of Organic Chemistry | 1998 |