引用本文: 
				
					Jian Hong Liu,  Dong Liang,  Bin Bin Fan,  Rui Feng Li,  Hua Chen. Enantioselective hydrogenation of acetophenone by (1S, 2S)-DPEN-Ru (Ⅱ) Cl2 (PPh3)2 encapsulated in Al-MCM-41[J]. Chinese Chemical Letters,
							2010, 21(7): 802-806.
							
							doi:
								10.1016/j.cclet.2010.03.011
						
					
				
					
				
			
			
Citation: Jian Hong Liu, Dong Liang, Bin Bin Fan, Rui Feng Li, Hua Chen. Enantioselective hydrogenation of acetophenone by (1S, 2S)-DPEN-Ru (Ⅱ) Cl2 (PPh3)2 encapsulated in Al-MCM-41[J]. Chinese Chemical Letters, 2010, 21(7): 802-806. doi: 10.1016/j.cclet.2010.03.011
				
			
			
		
				
			
			Citation: Jian Hong Liu, Dong Liang, Bin Bin Fan, Rui Feng Li, Hua Chen. Enantioselective hydrogenation of acetophenone by (1S, 2S)-DPEN-Ru (Ⅱ) Cl2 (PPh3)2 encapsulated in Al-MCM-41[J]. Chinese Chemical Letters, 2010, 21(7): 802-806. doi: 10.1016/j.cclet.2010.03.011
				
			
			Enantioselective hydrogenation of acetophenone by (1S, 2S)-DPEN-Ru (Ⅱ) Cl2 (PPh3)2 encapsulated in Al-MCM-41
								摘要:
								A chiral ruthenium complex [(1S,2S)-DPEN]-RuCl2 (PPh3)2 (DPEN=1,2-diphenylethylenediamine, PPh3=triphenylphosph-ine) was encapsulated in the channel of Al-MCM-41 by electrostatic adsorption and 1,1-dichlorosilacyclobutane modification. The prepared heterogeneous catalyst showed the same catalytic activity and enantioselectivity as the corresponding homogeneous catalyst in the asymmetric hydrogenation of acetophenone, and could be reused at least seven times without significant loss of catalytic activity and enantioselectivity.
						
						English
Enantioselective hydrogenation of acetophenone by (1S, 2S)-DPEN-Ru (Ⅱ) Cl2 (PPh3)2 encapsulated in Al-MCM-41
							Abstract:
								A chiral ruthenium complex [(1S,2S)-DPEN]-RuCl2 (PPh3)2 (DPEN=1,2-diphenylethylenediamine, PPh3=triphenylphosph-ine) was encapsulated in the channel of Al-MCM-41 by electrostatic adsorption and 1,1-dichlorosilacyclobutane modification. The prepared heterogeneous catalyst showed the same catalytic activity and enantioselectivity as the corresponding homogeneous catalyst in the asymmetric hydrogenation of acetophenone, and could be reused at least seven times without significant loss of catalytic activity and enantioselectivity.
						
						
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