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.
6. Nickel-catalyzed cross-coupling reactions of benzylic zinc reagents with aromatic bromides, chlorides and tosylates. Schade MA; Metzger A; Hug S; Knochel P Chem Commun (Camb); 2008 Jul; (26):3046-8. PubMed ID: 18688343 [TBL] [Abstract][Full Text] [Related]
7. Negishi cross-coupling reactions catalyzed by an aminophosphine-based nickel system: a reliable and general applicable reaction protocol for the high-yielding synthesis of biaryls. Gerber R; Frech CM Chemistry; 2011 Oct; 17(42):11893-904. PubMed ID: 21887715 [TBL] [Abstract][Full Text] [Related]
8. Simple amine/Pd(OAc)(2)-catalyzed suzuki coupling reactions of aryl bromides under mild aerobic conditions. Tao B; Boykin DW J Org Chem; 2004 Jun; 69(13):4330-5. PubMed ID: 15202886 [TBL] [Abstract][Full Text] [Related]
10. Guanidine/Pd(OAc)2-catalyzed room temperature Suzuki cross-coupling reaction in aqueous media under aerobic conditions. Li S; Lin Y; Cao J; Zhang S J Org Chem; 2007 May; 72(11):4067-72. PubMed ID: 17465565 [TBL] [Abstract][Full Text] [Related]
11. Efficient Negishi coupling reactions of aryl chlorides catalyzed by binuclear and mononuclear nickel-N-heterocyclic carbene complexes. Xi Z; Zhou Y; Chen W J Org Chem; 2008 Nov; 73(21):8497-501. PubMed ID: 18841915 [TBL] [Abstract][Full Text] [Related]
12. Nickel(II) complexes of bidentate N-heterocyclic carbene/phosphine ligands: efficient catalysts for Suzuki coupling of aryl chlorides. Lee CC; Ke WC; Chan KT; Lai CL; Hu CH; Lee HM Chemistry; 2007; 13(2):582-91. PubMed ID: 16969780 [TBL] [Abstract][Full Text] [Related]
13. Highly active palladium catalysts supported by bulky proazaphosphatrane ligands for Stille cross-coupling: coupling of aryl and vinyl chlorides, room temperature coupling of aryl bromides, coupling of aryl triflates, and synthesis of sterically hindered biaryls. Su W; Urgaonkar S; McLaughlin PA; Verkade JG J Am Chem Soc; 2004 Dec; 126(50):16433-9. PubMed ID: 15600345 [TBL] [Abstract][Full Text] [Related]
14. Homogeneous catalysts supported on soluble polymers: biphasic Sonogashira coupling of aryl halides and acetylenes using MeOPEG-bound phosphine-palladium catalysts for efficient catalyst recycling. Köllhofer A; Plenio H Chemistry; 2003 Mar; 9(6):1416-25. PubMed ID: 12645031 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Pd(PPh3)4-PEG 400 catalyzed protocol for the atom-efficient Stille cross-coupling reaction of organotin with aryl bromides. Zhou WJ; Wang KH; Wang JX J Org Chem; 2009 Aug; 74(15):5599-602. PubMed ID: 19552378 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Efficient Stille cross-coupling reaction catalyzed by the Pd(OAc)2/Dabco catalytic system. Li JH; Liang Y; Wang DP; Liu WJ; Xie YX; Yin DL J Org Chem; 2005 Apr; 70(7):2832-4. PubMed ID: 15787581 [TBL] [Abstract][Full Text] [Related]
19. Aqueous-phase, palladium-catalyzed cross-coupling of aryl bromides under mild conditions, using water-soluble, sterically demanding alkylphosphines. DeVasher RB; Moore LR; Shaughnessy KH J Org Chem; 2004 Nov; 69(23):7919-27. PubMed ID: 15527271 [TBL] [Abstract][Full Text] [Related]
20. A highly efficient catalytic system for cross-coupling of aryl chlorides and bromides with malononitrile anion by palladium carbene complexes. Gao C; Tao X; Qian Y; Huang J Chem Commun (Camb); 2003 Jun; (12):1444-5. PubMed ID: 12841283 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]