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.
5. 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]
6. Palladium-catalyzed cross-coupling reactions of heterocyclic silanolates with substituted aryl iodides and bromides. Denmark SE; Baird JD Org Lett; 2006 Feb; 8(4):793-5. PubMed ID: 16468769 [TBL] [Abstract][Full Text] [Related]
7. 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]
9. Oxidative addition of aryl tosylates to palladium(0) and coupling of unactivated aryl tosylates at room temperature. Roy AH; Hartwig JF J Am Chem Soc; 2003 Jul; 125(29):8704-5. PubMed ID: 12862447 [TBL] [Abstract][Full Text] [Related]
10. Cu-Catalyzed carbon-heteroatom coupling reactions under mild conditions promoted by resin-bound organic ionic bases. Huang YB; Yang CT; Yi J; Deng XJ; Fu Y; Liu L J Org Chem; 2011 Feb; 76(3):800-10. PubMed ID: 21194222 [TBL] [Abstract][Full Text] [Related]
11. Palladium-catalyzed Stille cross-couplings of sulfonyl chlorides and organostannanes. Dubbaka SR; Vogel P J Am Chem Soc; 2003 Dec; 125(50):15292-3. PubMed ID: 14664564 [TBL] [Abstract][Full Text] [Related]
12. Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides. Zhou JS; Fu GC J Am Chem Soc; 2003 Dec; 125(48):14726-7. PubMed ID: 14640646 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Novel class of tertiary phosphine ligands based on a phospha-adamantane framework and use in the Suzuki cross-coupling reactions of aryl halides under mild conditions. Adjabeng G; Brenstrum T; Wilson J; Frampton C; Robertson A; Hillhouse J; McNulty J; Capretta A Org Lett; 2003 Mar; 5(6):953-5. PubMed ID: 12633114 [TBL] [Abstract][Full Text] [Related]
15. Palladium-catalyzed cross-coupling reactions between dihydropyranylindium reagents and aryl halides. synthesis of C-aryl glycals. Lehmann U; Awasthi S; Minehan T Org Lett; 2003 Jul; 5(14):2405-8. PubMed ID: 12841741 [TBL] [Abstract][Full Text] [Related]
16. Palladium-catalyzed C(sp3)-H arylation of diarylmethanes at room temperature: synthesis of triarylmethanes via deprotonative-cross-coupling processes. Zhang J; Bellomo A; Creamer AD; Dreher SD; Walsh PJ J Am Chem Soc; 2012 Aug; 134(33):13765-72. PubMed ID: 22816972 [TBL] [Abstract][Full Text] [Related]
17. Synthesis of α,α-difluoromethylene alkynes by palladium-catalyzed gem-difluoropropargylation of aryl and alkenyl boron reagents. Yu YB; He GZ; Zhang X Angew Chem Int Ed Engl; 2014 Sep; 53(39):10457-61. PubMed ID: 25078096 [TBL] [Abstract][Full Text] [Related]
18. Base-Activated Latent Heteroaromatic Sulfinates as Nucleophilic Coupling Partners in Palladium-Catalyzed Cross-Coupling Reactions. Cook XAF; Pantaine LRE; Blakemore DC; Moses IB; Sach NW; Shavnya A; Willis MC Angew Chem Int Ed Engl; 2021 Oct; 60(41):22461-22468. PubMed ID: 34342107 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]