[2,6-双[(二-1-哌啶基膦)氨基]苯基]氯化钯(II)
![[2,6-双[(二-1-哌啶基膦)氨基]苯基]氯化钯(II)结构式](https://image.chemsrc.com/caspic/466/955035-37-7.png)
[2,6-双[(二-1-哌啶基膦)氨基]苯基]氯化钯(II)结构式
|
常用名 | [2,6-双[(二-1-哌啶基膦)氨基]苯基]氯化钯(II) | 英文名 | (2,6-Bis((di(piperidin-1-yl)phosphino)amino)phenyl)palladium(II) chloride |
|---|---|---|---|---|
| CAS号 | 955035-37-7 | 分子量 | 645.49600 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C26H45ClN6P2Pd | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | N/A | |
| 符号 |
GHS07 |
信号词 | Warning |
|
Comparative Study of the Frech Catalyst with Two Conventional Catalysts in the Heck Synthesis of 2,4-Diaminopyrimidine-based Antibiotics.
Org. Prep. Proced. Int. 45(1) , 66-71, (2013)
|
|
|
Short, facile, and high-yielding synthesis of extremely efficient pincer-type suzuki catalysts bearing aminophosphine substituents.
Angew. Chem. Int. Ed. Engl. 46 , 6514-6517, (2007)
|
|
|
Rationally designed pincer-type heck catalysts bearing aminophosphine substituents: Pd IV intermediates and palladium nanoparticles.
Chemistry 14 , 7969-7977, (2008) The aminophosphine-based pincer complexes [C6H3-2,6-(XP(piperidinyl)2)2Pd(Cl)] (X=NH 1; X=O 2) are readily prepared from cheap starting materials by sequential addition of 1,1',1''-phosphinetriyltripiperidine and 1,3-diaminobenzene or resorcinol to solutions ... |
|
|
Bolliger, J. L. and Frech,C. M.
Adv. Synth. Catal. 351 , 891-902, (2009)
|
|
|
Bolliger, J. L. and Frech,C. M.,
Adv. Synth. Catal. 352 , 1075-1080, (2010)
|
|
|
Aminophosphine palladium pincer complexes for Suzuki and Heck reactions. Bolliger, J. L., and Frech, C. M.
Chimia 63 , 23, (2009)
|