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Journal Abstract Search
176 related items for PubMed ID: 21916501
1. Nickel-catalyzed asymmetric α-arylation and heteroarylation of ketones with chloroarenes: effect of halide on selectivity, oxidation state, and room-temperature reactions. Ge S, Hartwig JF. J Am Chem Soc; 2011 Oct 19; 133(41):16330-3. PubMed ID: 21916501 [Abstract] [Full Text] [Related]
2. Controlling first-row catalysts: amination of aryl and heteroaryl chlorides and bromides with primary aliphatic amines catalyzed by a BINAP-ligated single-component Ni(0) complex. Ge S, Green RA, Hartwig JF. J Am Chem Soc; 2014 Jan 29; 136(4):1617-27. PubMed ID: 24397570 [Abstract] [Full Text] [Related]
3. Nickel-catalyzed reductive coupling of aryl halides with secondary alkyl bromides and allylic acetate. Wang S, Qian Q, Gong H. Org Lett; 2012 Jul 06; 14(13):3352-5. PubMed ID: 22697415 [Abstract] [Full Text] [Related]
4. General and mild Ni(0)-catalyzed α-arylation of ketones using aryl chlorides. Fernández-Salas JA, Marelli E, Cordes DB, Slawin AM, Nolan SP. Chemistry; 2015 Mar 02; 21(10):3906-9. PubMed ID: 25611197 [Abstract] [Full Text] [Related]
5. Room-temperature Kumada cross-coupling of unactivated aryl chlorides catalyzed by N-heterocylic carbene-based nickel(II) complexes. Xi Z, Liu B, Chen W. J Org Chem; 2008 May 16; 73(10):3954-7. PubMed ID: 18412386 [Abstract] [Full Text] [Related]
6. Pd-catalyzed α-arylation of α,α-difluoroketones with aryl bromides and chlorides. A route to difluoromethylarenes. Ge S, Chaładaj W, Hartwig JF. J Am Chem Soc; 2014 Mar 19; 136(11):4149-52. PubMed ID: 24588379 [Abstract] [Full Text] [Related]
11. Palladium-catalyzed C-H functionalization of heteroarenes with aryl bromides and chlorides. Tamba S, Okubo Y, Tanaka S, Monguchi D, Mori A. J Org Chem; 2010 Oct 15; 75(20):6998-7001. PubMed ID: 20857989 [Abstract] [Full Text] [Related]
17. An improved palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides. Pan J, Wang X, Zhang Y, Buchwald SL. Org Lett; 2011 Sep 16; 13(18):4974-6. PubMed ID: 21863838 [Abstract] [Full Text] [Related]