(2,6-Bis((di(piperidin-1-yl)phosphino)amino)phenyl)palladium(II) chloride
(2,6-Bis((di(piperidin-1-yl)phosphino)amino)phenyl)palladium(II) chloride structure
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Common Name | (2,6-Bis((di(piperidin-1-yl)phosphino)amino)phenyl)palladium(II) chloride | ||
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| CAS Number | 955035-37-7 | Molecular Weight | 645.49600 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C26H45ClN6P2Pd | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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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)
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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)
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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 ... |
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Bolliger, J. L. and Frech,C. M.
Adv. Synth. Catal. 351 , 891-902, (2009)
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Bolliger, J. L. and Frech,C. M.,
Adv. Synth. Catal. 352 , 1075-1080, (2010)
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Aminophosphine palladium pincer complexes for Suzuki and Heck reactions. Bolliger, J. L., and Frech, C. M.
Chimia 63 , 23, (2009)
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