These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
502 related articles for article (PubMed ID: 23460083)
1. Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. Han FS Chem Soc Rev; 2013 Jun; 42(12):5270-98. PubMed ID: 23460083 [TBL] [Abstract][Full Text] [Related]
2. Exploration of new C-O electrophiles in cross-coupling reactions. Yu DG; Li BJ; Shi ZJ Acc Chem Res; 2010 Dec; 43(12):1486-95. PubMed ID: 20849101 [TBL] [Abstract][Full Text] [Related]
3. The promise and challenge of iron-catalyzed cross coupling. Sherry BD; Fürstner A Acc Chem Res; 2008 Nov; 41(11):1500-11. PubMed ID: 18588321 [TBL] [Abstract][Full Text] [Related]
4. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters. Tollefson EJ; Hanna LE; Jarvo ER Acc Chem Res; 2015 Aug; 48(8):2344-53. PubMed ID: 26197033 [TBL] [Abstract][Full Text] [Related]
5. Nickel catalyzed cross-coupling of aryl C-O based electrophiles with aryl neopentylglycolboronates. Leowanawat P; Zhang N; Percec V J Org Chem; 2012 Jan; 77(2):1018-25. PubMed ID: 22263719 [TBL] [Abstract][Full Text] [Related]
6. Nickel-catalyzed Suzuki-Miyaura reaction of aryl fluorides. Tobisu M; Xu T; Shimasaki T; Chatani N J Am Chem Soc; 2011 Dec; 133(48):19505-11. PubMed ID: 22023167 [TBL] [Abstract][Full Text] [Related]
7. Exploration of earth-abundant transition metals (Fe, Co, and Ni) as catalysts in unreactive chemical bond activations. Su B; Cao ZC; Shi ZJ Acc Chem Res; 2015 Mar; 48(3):886-96. PubMed ID: 25679917 [TBL] [Abstract][Full Text] [Related]
8. Comparison of arylboron-based nucleophiles in Ni-catalyzed Suzuki-Miyaura cross-coupling with aryl mesylates and sulfamates. Zhang N; Hoffman DJ; Gutsche N; Gupta J; Percec V J Org Chem; 2012 Jul; 77(14):5956-64. PubMed ID: 22712768 [TBL] [Abstract][Full Text] [Related]
12. Pd-Catalyzed Suzuki-Miyaura Cross-Coupling of Pentafluorophenyl Esters. Buchspies J; J Pyle D; He H; Szostak M Molecules; 2018 Nov; 23(12):. PubMed ID: 30501083 [TBL] [Abstract][Full Text] [Related]
13. Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions. Rudolph A; Lautens M Angew Chem Int Ed Engl; 2009; 48(15):2656-70. PubMed ID: 19173365 [TBL] [Abstract][Full Text] [Related]
14. Bis-diimidazolylidine complexes of nickel: investigations into nickel catalyzed coupling reactions. Paulose TA; Wu SC; Olson JA; Chau T; Theaker N; Hassler M; Quail JW; Foley SR Dalton Trans; 2012 Jan; 41(1):251-60. PubMed ID: 22020444 [TBL] [Abstract][Full Text] [Related]
15. Transmetalation in the Suzuki-Miyaura coupling: the fork in the trail. Lennox AJ; Lloyd-Jones GC Angew Chem Int Ed Engl; 2013 Jul; 52(29):7362-70. PubMed ID: 23780626 [TBL] [Abstract][Full Text] [Related]
16. Well-Defined Palladium(II)-NHC Precatalysts for Cross-Coupling Reactions of Amides and Esters by Selective N-C/O-C Cleavage. Shi S; Nolan SP; Szostak M Acc Chem Res; 2018 Oct; 51(10):2589-2599. PubMed ID: 30240190 [TBL] [Abstract][Full Text] [Related]
17. Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s). Terao J; Kambe N Acc Chem Res; 2008 Nov; 41(11):1545-54. PubMed ID: 18973349 [TBL] [Abstract][Full Text] [Related]
18. Organogold reactivity with palladium, nickel, and rhodium: transmetalation, cross-coupling, and dual catalysis. Hirner JJ; Shi Y; Blum SA Acc Chem Res; 2011 Aug; 44(8):603-13. PubMed ID: 21644576 [TBL] [Abstract][Full Text] [Related]
19. Rapid nickel-catalyzed Suzuki-Miyaura cross-couplings of aryl carbamates and sulfamates utilizing microwave heating. Baghbanzadeh M; Pilger C; Kappe CO J Org Chem; 2011 Mar; 76(5):1507-10. PubMed ID: 21250707 [TBL] [Abstract][Full Text] [Related]
20. Mechanistic insights into nickamine-catalyzed alkyl-alkyl cross-coupling reactions. Breitenfeld J; Hu X Chimia (Aarau); 2014; 68(4):235-8. PubMed ID: 24983605 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]