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.
63. A copper- and amine-free sonogashira reaction employing aminophosphines as ligands. Cheng J; Sun Y; Wang F; Guo M; Xu JH; Pan Y; Zhang Z J Org Chem; 2004 Aug; 69(16):5428-32. PubMed ID: 15287792 [TBL] [Abstract][Full Text] [Related]
64. Pd/C-catalyzed, copper-free Sonogashira coupling: one-pot synthesis of 1-aryl-4-(2-phenylethynyl)[1,2,4]triazolo[4,3- Bakherad M; Jajarmi S Monatsh Chem; 2013; 144(6):885-890. PubMed ID: 26166882 [TBL] [Abstract][Full Text] [Related]
65. Rapid room temperature Buchwald-Hartwig and Suzuki-Miyaura couplings of heteroaromatic compounds employing low catalyst loadings. Navarro O; Marion N; Mei J; Nolan SP Chemistry; 2006 Jun; 12(19):5142-8. PubMed ID: 16628762 [TBL] [Abstract][Full Text] [Related]
66. One-Pot Synthesis of (Z)-β-Halovinyl Ketones via the Cascade of Sonogashira Coupling and Hydrohalogenation. Chen FJ; Hua Z; Chen J; Chen J; Lee D; Xia Y Front Chem; 2020; 8():621545. PubMed ID: 33968892 [TBL] [Abstract][Full Text] [Related]
67. Copper-free sonogashira coupling reaction with PdCl2 in water under aerobic conditions. Liang B; Dai M; Chen J; Yang Z J Org Chem; 2005 Jan; 70(1):391-3. PubMed ID: 15624959 [TBL] [Abstract][Full Text] [Related]
68. Heterogeneous versus homogeneous palladium catalysts for ligandless mizoroki-heck reactions: a comparison of batch/microwave and continuous-flow processing. Glasnov TN; Findenig S; Kappe CO Chemistry; 2009; 15(4):1001-10. PubMed ID: 19086042 [TBL] [Abstract][Full Text] [Related]
69. Assemblies of Copper Ferrite and Palladium Nanoparticles on Silica Microparticles as a Magnetically Recoverable Catalyst for Sonogashira Reaction under Mild Conditions. Gholinejad M; Ahmadi J Chempluschem; 2015 Jun; 80(6):973-979. PubMed ID: 31973253 [TBL] [Abstract][Full Text] [Related]
70. Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides. Littke AF; Schwarz L; Fu GC J Am Chem Soc; 2002 Jun; 124(22):6343-8. PubMed ID: 12033863 [TBL] [Abstract][Full Text] [Related]
76. The first applications of carbene ligands in cross-couplings of alkyl electrophiles: sonogashira reactions of unactivated alkyl bromides and iodides. Eckhardt M; Fu GC J Am Chem Soc; 2003 Nov; 125(45):13642-3. PubMed ID: 14599185 [TBL] [Abstract][Full Text] [Related]
77. Pd-tetrahydrosalan-type complexes as catalysts for sonogashira couplings in water: efficient greening of the procedure. Voronova K; Homolya L; Udvardy A; Bényei AC; Joó F ChemSusChem; 2014 Aug; 7(8):2230-9. PubMed ID: 24995656 [TBL] [Abstract][Full Text] [Related]
78. Rapid access to unsymmetrical tolanes and alkynones by sequentially palladium-catalyzed one-pot processes. Götzinger AC; Müller TJ Org Biomol Chem; 2016 Apr; 14(14):3498-500. PubMed ID: 26988334 [TBL] [Abstract][Full Text] [Related]
79. Efficient copper-free PdCl2(PCy3)2-catalyzed Sonogashira coupling of aryl chlorides with terminal alkynes. Yi C; Hua R J Org Chem; 2006 Mar; 71(6):2535-7. PubMed ID: 16526813 [TBL] [Abstract][Full Text] [Related]
80. Modified (NHC)Pd(allyl)Cl (NHC = N-heterocyclic carbene) complexes for room-temperature Suzuki-Miyaura and Buchwald-Hartwig reactions. Marion N; Navarro O; Mei J; Stevens ED; Scott NM; Nolan SP J Am Chem Soc; 2006 Mar; 128(12):4101-11. PubMed ID: 16551119 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]