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.
9. A study on applications of N-substituted main-chain NHC-palladium polymers as recyclable self-supported catalysts for the Suzuki-Miyaura coupling of aryl chlorides in water. Karimi B; Akhavan PF Inorg Chem; 2011 Jul; 50(13):6063-72. PubMed ID: 21648445 [TBL] [Abstract][Full Text] [Related]
10. Practical and efficient Suzuki-Miyaura cross-coupling of 2-iodocycloenones with arylboronic acids catalyzed by recyclable Pd(0)/C. Felpin FX J Org Chem; 2005 Oct; 70(21):8575-8. PubMed ID: 16209612 [TBL] [Abstract][Full Text] [Related]
11. Practical preparation method of polymer-incarcerated (PI) palladium catalysts using Pd(II) salts. Hagio H; Sugiura M; Kobayashi S Org Lett; 2006 Feb; 8(3):375-8. PubMed ID: 16435838 [TBL] [Abstract][Full Text] [Related]
12. Supported ionic liquid catalyst (Pd-SILC) for highly efficient and recyclable Suzuki-Miyaura reaction. Hagiwara H; Ko KH; Hoshi T; Suzuki T Chem Commun (Camb); 2007 Jul; (27):2838-40. PubMed ID: 17609793 [TBL] [Abstract][Full Text] [Related]
13. Facile synthesis of highly stable gold nanoparticles and their unexpected excellent catalytic activity for Suzuki-Miyaura cross-coupling reaction in water. Han J; Liu Y; Guo R J Am Chem Soc; 2009 Feb; 131(6):2060-1. PubMed ID: 19170490 [TBL] [Abstract][Full Text] [Related]
14. Pyridyl-supported pyrazolyl-N-heterocyclic carbene ligands and the catalytic activity of their palladium complexes in Suzuki-Miyaura reactions. Zeng F; Yu Z J Org Chem; 2006 Jul; 71(14):5274-81. PubMed ID: 16808516 [TBL] [Abstract][Full Text] [Related]
15. New catalysts for Suzuki-Miyaura coupling reactions of heteroatom-substituted heteroaryl chlorides. Guram AS; Wang X; Bunel EE; Faul MM; Larsen RD; Martinelli MJ J Org Chem; 2007 Jul; 72(14):5104-12. PubMed ID: 17550290 [TBL] [Abstract][Full Text] [Related]
16. Highly active oxime-derived palladacycle complexes for Suzuki-Miyaura and Ullmann-type coupling reactions. Alonso DA; Nájera C; Pacheco MC J Org Chem; 2002 Aug; 67(16):5588-94. PubMed ID: 12153256 [TBL] [Abstract][Full Text] [Related]
17. Suzuki-Miyaura, alpha-ketone arylation and dehalogenation reactions catalyzed by a versatile N-heterocyclic carbene-palladacycle complex. Navarro O; Marion N; Oonishi Y; Kelly RA; Nolan SP J Org Chem; 2006 Jan; 71(2):685-92. PubMed ID: 16408981 [TBL] [Abstract][Full Text] [Related]
18. Triazole-based monophosphines for Suzuki-Miyaura coupling and amination reactions of aryl chlorides. Liu D; Gao W; Dai Q; Zhang X Org Lett; 2005 Oct; 7(22):4907-10. PubMed ID: 16235919 [TBL] [Abstract][Full Text] [Related]
19. Generation of an aromatic amide-derived phosphane (Aphos) library by self-assisted molecular editing and applications of Aphos in room-temperature Suzuki-Miyaura reactions. Dai WM; Li Y; Zhang Y; Yue C; Wu J Chemistry; 2008; 14(18):5538-54. PubMed ID: 18478517 [TBL] [Abstract][Full Text] [Related]
20. Ordered mesoporous organosilica with ionic-liquid framework: an efficient and reusable support for the palladium-catalyzed Suzuki-Miyaura coupling reaction in water. Karimi B; Elhamifar D; Clark JH; Hunt AJ Chemistry; 2010 Jul; 16(27):8047-53. PubMed ID: 20512825 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]