Citation:
	            
		            Zan Liu,  Xiaolei Nan,  Tao Lei,  Chao Zhou,  Yang Wang,  Wenqiang Liu,  Bin Chen,  Chenho Tung,  Lizhu Wu. Photo-induced reductive cross-coupling of aldehydes, ketones and imines with electron-deficient arenes to construct aryl substituted alcohols and amines[J]. Chinese Journal of Catalysis,
							;2018, 39(3): 487-494.
						
							doi:
								10.1016/S1872-2067(17)62896-1
						
					
				
					
				
	        
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	                	Umpolung reactions of C=X bonds (X=O, N) are valuable ways of constructing new C-C bonds, which are sometimes difficult to be constructed using traditional synthetic pathways. Classical polarity inversion of C=X bonds (X=O, N) usually requires air or moisture-sensitive and strong reducing agents, which limit the feasibility of substrate scope. Herein we describe a photo-induced reductive cross-coupling reaction of aldehydes, ketones and imines with electron-deficient arenes (aromatic nitriles) using fac-Ir(ppy)3 as a photocatalyst and diisopropylethylamine (DIPEA) as a terminal reductant under visible light irradiation. Mild conditions and high yields mean that this new polarity inversion strategy can be used with aryl-substituted alcohols and amines. Spectroscopic studies and control experiments have demonstrated the oxidative quenching of Ir(ppy)3* by electron-deficient arenes involved in the key step for the C-C bond formation.
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