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.
278 related articles for article (PubMed ID: 19322847)
1. A general palladium-catalyzed amination of aryl halides with ammonia. Schulz T; Torborg C; Enthaler S; Schäffner B; Dumrath A; Spannenberg A; Neumann H; Börner A; Beller M Chemistry; 2009; 15(18):4528-33. PubMed ID: 19322847 [TBL] [Abstract][Full Text] [Related]
2. Palladium-catalyzed aminations of aryl halides with phosphine-functionalized imidazolium ligands. Shi JC; Yang P; Tong Q; Jia L Dalton Trans; 2008 Feb; (7):938-45. PubMed ID: 18259628 [TBL] [Abstract][Full Text] [Related]
3. Application of a new bicyclic triaminophosphine ligand in Pd-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides, bromides, and iodides. Urgaonkar S; Xu JH; Verkade JG J Org Chem; 2003 Oct; 68(22):8416-23. PubMed ID: 14575466 [TBL] [Abstract][Full Text] [Related]
4. Sterically bulky thioureas as air- and moisture-stable ligands for pd-catalyzed Heck reactions of aryl halides. Yang D; Chen YC; Zhu NY Org Lett; 2004 May; 6(10):1577-80. PubMed ID: 15128240 [TBL] [Abstract][Full Text] [Related]
5. Homogeneous catalysts supported on soluble polymers: biphasic Suzuki-Miyaura coupling of aryl chlorides using phase-tagged palladium-phosphine catalysts. an der Heiden M; Plenio H Chemistry; 2004 Apr; 10(7):1789-97. PubMed ID: 15054766 [TBL] [Abstract][Full Text] [Related]
6. BippyPhos: a single ligand with unprecedented scope in the Buchwald-Hartwig amination of (hetero)aryl chlorides. Crawford SM; Lavery CB; Stradiotto M Chemistry; 2013 Dec; 19(49):16760-71. PubMed ID: 24281816 [TBL] [Abstract][Full Text] [Related]
7. Palladium-catalyzed amination of aryl halides on solid support. Weigand K; Pelka S Org Lett; 2002 Dec; 4(26):4689-92. PubMed ID: 12489962 [TBL] [Abstract][Full Text] [Related]
8. (t-Bu)2PN=P(i-BuNCH2CH2)3N: new efficient ligand for palladium-catalyzed C-N couplings of aryl and heteroaryl bromides and chlorides and for vinyl bromides at room temperature. Reddy ChV; Kingston JV; Verkade JG J Org Chem; 2008 Apr; 73(8):3047-62. PubMed ID: 18370424 [TBL] [Abstract][Full Text] [Related]
9. 9-fluorenylphosphines for the Pd-catalyzed sonogashira, suzuki, and Buchwald-Hartwig coupling reactions in organic solvents and water. Fleckenstein CA; Plenio H Chemistry; 2007; 13(9):2701-16. PubMed ID: 17200923 [TBL] [Abstract][Full Text] [Related]
10. Bulky alkylphosphines with neopentyl substituents as ligands in the amination of aryl bromides and chlorides. Hill LL; Moore LR; Huang R; Craciun R; Vincent AJ; Dixon DA; Chou J; Woltermann CJ; Shaughnessy KH J Org Chem; 2006 Jul; 71(14):5117-25. PubMed ID: 16808497 [TBL] [Abstract][Full Text] [Related]
11. Easily accessible and highly tunable indolyl phosphine ligands for Suzuki-Miyaura coupling of aryl chlorides. So CM; Lau CP; Kwong FY Org Lett; 2007 Jul; 9(15):2795-8. PubMed ID: 17602563 [TBL] [Abstract][Full Text] [Related]
12. Palladium-catalyzed tetrakis(dimethylamino)ethylene-promoted reductive coupling of aryl halides. Kuroboshi M; Waki Y; Tanaka H J Org Chem; 2003 May; 68(10):3938-42. PubMed ID: 12737575 [TBL] [Abstract][Full Text] [Related]
13. Highly active palladium/activated carbon catalysts for Heck reactions: correlation of activity, catalyst properties, and Pd leaching. Köhler K; Heidenreich RG; Krauter JG; Pietsch J Chemistry; 2002 Feb; 8(3):622-31. PubMed ID: 11859857 [TBL] [Abstract][Full Text] [Related]
14. Macroporous polystyrene-supported palladium catalyst containing a bulky N-heterocyclic carbene ligand for Suzuki reaction of aryl chlorides. Lee DH; Kim JH; Jun BH; Kang H; Park J; Lee YS Org Lett; 2008 Apr; 10(8):1609-12. PubMed ID: 18351771 [TBL] [Abstract][Full Text] [Related]
15. Progress in the palladium-catalyzed cyanation of aryl chlorides. Sundermeier M; Zapf A; Mutyala S; Baumann W; Sans J; Weiss S; Beller M Chemistry; 2003 Apr; 9(8):1828-36. PubMed ID: 12698441 [TBL] [Abstract][Full Text] [Related]
16. New ligands for a general palladium-catalyzed amination of aryl and heteroaryl chlorides. Rataboul F; Zapf A; Jackstell R; Harkal S; Riermeier T; Monsees A; Dingerdissen U; Beller M Chemistry; 2004 Jun; 10(12):2983-90. PubMed ID: 15214081 [TBL] [Abstract][Full Text] [Related]
17. Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: scope and structure-activity relationships. Shen Q; Ogata T; Hartwig JF J Am Chem Soc; 2008 May; 130(20):6586-96. PubMed ID: 18444639 [TBL] [Abstract][Full Text] [Related]
18. Solvent free amination reactions of aryl bromides at room temperature catalyzed by a (pi-allyl)palladium complex bearing a diphosphinidenecyclobutene ligand. Gajare AS; Toyota K; Yoshifuji M; Ozawa F J Org Chem; 2004 Sep; 69(19):6504-6. PubMed ID: 15357620 [TBL] [Abstract][Full Text] [Related]
19. Scope and limitations of Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides. Urgaonkar S; Verkade JG J Org Chem; 2004 Dec; 69(26):9135-42. PubMed ID: 15609947 [TBL] [Abstract][Full Text] [Related]
20. Palladium-catalyzed alpha-arylation of tetramic acids. Storgaard M; Dörwald FZ; Peschke B; Tanner D J Org Chem; 2009 Jul; 74(14):5032-40. PubMed ID: 19472991 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]