[Pd(dppp)(H2O)2](BF4)2
2 Structure](https://image.chemsrc.com/caspic/066/134668-73-8.png)
[Pd(dppp)(H2O)2](BF4)2 structure
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Common Name | [Pd(dppp)(H2O)2](BF4)2 | ||
|---|---|---|---|---|
| CAS Number | 134668-73-8 | Molecular Weight | 641.71 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C27H30BF4O2P2Pd+ | Melting Point | 175-200°C (decomposition) | |
| MSDS | USA | Flash Point | N/A | |
| Name | [Pd(dppp)(H2O)2](BF4)2 |
|---|
| Melting Point | 175-200°C (decomposition) |
|---|---|
| Molecular Formula | C27H30BF4O2P2Pd+ |
| Molecular Weight | 641.71 |
| RIDADR | NONH for all modes of transport |
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Cationic palladium complex catalyzed diastereo- and enantioselective tandem annulation of 2-formylarylboronic acids with allenoates.
Org. Lett. 11 , 4366-4369, (2009) Cationic palladium complex [(dppp)Pd(H(2)O)(2)](2+)(BF(4)(-))(2) catalyzed tandem annulation reactions of 2-formylarylboronic acids and allenoates produce the indenol derivatives diastereo- and enanti... |
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Cationic Pd(II)-catalyzed highly enantioselective arylative cyclization of alkyne-tethered enals or enones initiated by carbopalladation of alkynes with arylboronic acids.
Org. Lett. 7th ed., 14 , 1756-1759, (2012) Cationic Pd(II)-catalyzed enantioselective arylative cyclization of alkyne-tethered enals or enones initiated by carbopalladation of alkynes was developed without the necessity of a redox system. |
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Control of chemoselectivity by counteranions of cationic palladium complexes: a convenient enantioselective synthesis of dihydrocoumarins.
Org. Lett. 12 , 108, (2010) High chemoselectivity for the synthesis of two kinds of substituted coumarins controlled by the counteranions of the cationic palladium catalysts is described. The asymmetric version of the reaction f... |