Pure and Applied Chemistry

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• Zheng Xingliang, Yang Luo, Du Weiyuan, Ding Aishun, Guo Hao: Amine-Catalyzed Direct Photoarylation of Unactivated Arenes. Chem. Asian J. 2014, 9, 439. <http://dx.doi.org/10.1002/asia.201301371>
• Parkan Kamil, Pohl Radek, Kotora Martin: Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin. Chem. Eur. J. 2014, n/a. <http://dx.doi.org/10.1002/chem.201304304>
• Kumar Arun, Rao Gyandshwar Kumar, Saleem Fariha, Kumar Rupesh, Singh Ajai K.: Efficient catalysis of Suzuki–Miyaura CC coupling reactions with palladium(II) complexes of partially hydrolyzed bisimine ligands: A process important in environment context. Journal of Hazardous Materials 2014, 269, 9. <http://dx.doi.org/10.1016/j.jhazmat.2013.11.024>
• Song Juanjuan, Li Xinjian, Liang Apeng, Li Jingya, Zou Dapeng, Wu Yangjie, Wu Yusheng: Synthesis of aryloxyazetidines derivatives by CuI/L-proline catalyzed coupling reaction of arylboronic acid with 1-Boc-3-iodoazetidine. Tetrahedron Letters 2014. <http://dx.doi.org/10.1016/j.tetlet.2014.02.098>
• Al-Masoudi Najim A., Kassim Ali G., Abdul-Reda Nabeel A.: Synthesis of Potential Pyrimidine Derivatives via Suzuki Cross-Coupling Reaction as HIV and Kinesin Eg5 Inhibitors. Nucleosides, Nucleotides and Nucleic Acids 2014, 33, 141. <http://dx.doi.org/10.1080/15257770.2014.880475>
• Amatore Christian, Le Duc Gaëtan, Jutand Anny: Mechanism of Palladium-Catalyzed Suzuki-Miyaura Reactions: Multiple and Antagonistic Roles of Anionic “Bases” and Their Countercations. Chem. Eur. J. 2013, 19, 10082. <http://dx.doi.org/10.1002/chem.201300177>
• Khotina Irina A., Consonni Roberto, Kushakova Natalia S., Porzio William, Giovanella Umberto, Kovalev Alexey I., Babushkina Marina A., Peregudov Alexander S., Destri Silvia: Branched polyphenylenes and phenylene dendrimers: NMR and optical studies. European Polymer Journal 2013, 49, 4224. <http://dx.doi.org/10.1016/j.eurpolymj.2013.10.002>
• Trivedi Manoj, Singh Gurmeet, Nagarajan R., Rath Nigam P.: Imidazole containing palladium(II) complexes as efficient pre-catalyst systems for Heck and Suzuki coupling reaction: Synthesis, structural characterization and catalytic properties. Inorganica Chimica Acta 2013, 394, 107. <http://dx.doi.org/10.1016/j.ica.2012.08.003>
• Rivera José María, Colorado-Peralta Raúl, Ramírez Daniel J., Sanchez Mario, Sanchez-Castro Maria Esther: Synthesis, characterization, X-ray studies and DFT calculations of fused five–six and seven–six membered ring of new heterobicyclic system of boron compounds. Journal of Molecular Structure 2013, 1052, 24. <http://dx.doi.org/10.1016/j.molstruc.2013.08.039>
• Saleem Fariha, Rao Gyandshwar Kumar, Singh Pradhumn, Singh Ajai Kumar: Chalcogen-Dependent Palladation at the Benzyl Carbon of 2,3-Bis[(phenylchalcogeno)methyl]quinoxaline: Palladium Complexes Catalyzing Suzuki–Miyaura Coupling via Palladium–Chalcogen Nanoparticles. Organometallics 2013, 32, 387. <http://dx.doi.org/10.1021/om3006273>
• Pikul Stanislaw, Cheng Hua, Cheng Allen, Huang C. D., Ke Alex, Kuo LungHuang, Thompson Andrew, Wilder Susan: Synthetic Process Development of BMS-599793 Including Azaindole Negishi Coupling on Kilogram Scale. Org. Process Res. Dev. 2013, 17, 907. <http://dx.doi.org/10.1021/op400012p>
• Neu Rebecca C., Jiang Chunfang, Stephan Douglas W.: Bulky derivatives of boranes, boronic acids and boronate esters via reaction with diazomethanes. Dalton Trans. 2013, 42, 726. <http://dx.doi.org/10.1039/c2dt31868g>
• Sharma Kamal Nayan, Joshi Hemant, Singh Ved Vati, Singh Pradhumn, Singh Ajai Kumar: Palladium(ii) complexes of pyrazolated thio/selenoethers: syntheses, structures, single source precursors of Pd4Se and PdSe nano-particles and potential for catalyzing Suzuki–Miyaura coupling. Dalton Trans. 2013, 42, 3908. <http://dx.doi.org/10.1039/c2dt31975f>
• Ekkert Olga, Tuschewitzki Ottmar, Daniliuc Constantin G., Kehr Gerald, Erker Gerhard: Reaction of strongly electrophilic alkenylboranes with phosphanylalkynes: rare examples of intermolecular 1,1-alkenylboration reactions. Chem. Commun. 2013, 49, 6992. <http://dx.doi.org/10.1039/c3cc43294g>
• Verma Sanny, Le Bras Jean, Jain Suman L., Muzart Jacques: Nanocrystalline starch grafted palladium(ii) complex for the Mizoroki–Heck reaction. Dalton Trans. 2013, 42, 14454. <http://dx.doi.org/10.1039/c3dt51685g>
• Kim Woo Yeon, Yoon Keun-Byoung: Synthesis of Novel Carbazole-based Blue Light-emitting Copolymers Containing (Diphenylene)vinylene Pendants. Polymer Korea 2013, 37, 736. <http://dx.doi.org/10.7317/pk.2013.37.6.736>
• Hajipour Abdol R., Karami Kazem, Tavakoli Ghazal: A comparative Suzuki reaction of aryl halides using a new dimeric orthopalladated complex under conventional and microwave irradiation conditions. Appl. Organometal. Chem. 2012, 26, 401. <http://dx.doi.org/10.1002/aoc.2852>
• Hajipour Abdol Reza, Dehbane Ifa Mahboobi, Rafiee Fatemeh: Synthesis of a new palladium salt using N -benzyl DABCO chloride and its application in Suzuki reaction. Appl. Organometal. Chem. 2012, 26, 743. <http://dx.doi.org/10.1002/aoc.2926>
• Gurram Venkateshwarlu, Pottabathini Narender, Garlapati Ramesh, Chaudhary Avinash B., Patro Balaram, Lakshman Mahesh K.: CC Cross-Coupling Reactions of O6-Alkyl-2-Haloinosine Derivatives and a One-Pot Cross-Coupling/O6-Deprotection Procedure. Chem. Asian J. 2012, 7, 1853. <http://dx.doi.org/10.1002/asia.201200093>
• Amatore Christian, Jutand Anny, Le Duc Gaëtan: Mechanistic Origin of Antagonist Effects of Usual Anionic Bases (OH− , CO3 2− ) as Modulated by their Countercations (Na+ , Cs+ , K+ ) in Palladium-Catalyzed Suzuki-Miyaura Reactions. Chem. Eur. J. 2012, 18, 6616. <http://dx.doi.org/10.1002/chem.201200516>
• Cui Jian-Fang, Chen Chao, Gao Xiang, Cai Zong-Wei, Han Jian-Wei, Wong Henry N. C.: 2,3,10,11-Tetrahydroxytetraphenylene and Its Application in Molecular Recognition. HCA 2012, 95, 2604. <http://dx.doi.org/10.1002/hlca.201200485>
• Andrews Martin J.I., Andrew Clase J., Bar Gregory, Tricarico Giovanni, Edwards Paul J., Brys Reginald, Chambers Mark, Schmidt Wolfgang, MacLeod Angus, Hirst Kim: Discovery of a series of imidazopyrazine small molecule inhibitors of the kinase MAPKAPK5, that show activity using in vitro and in vivo models of rheumatoid arthritis. Bioog Med Chem Lett 2012, 22, 2266. <http://dx.doi.org/10.1016/j.bmcl.2012.01.077>
• Domènech B., Muñoz M., Muraviev D.N., Macanás J.: Catalytic membranes with palladium nanoparticles: From tailored polymer to catalytic applications. Catalysis Today 2012, 193, 158. <http://dx.doi.org/10.1016/j.cattod.2012.02.049>
• Nasybulin Eduard, de Albuquerque Ian, Levon Kalle: Electrochemical synthesis of oligothiophenes by radical termination of the growing macromolecular chain. Elctrochim Acta 2012, 63, 341. <http://dx.doi.org/10.1016/j.electacta.2011.12.114>
• Rivera José María, Méndez Enrique, Colorado-Peralta Raúl, Rincón Susana, Farfán Norberto, Santillán Rosa: Synthesis, characterization and X-ray studies of new six–seven membered rings [4.5.0] heterobicyclic system of monomeric boronates. Inorganica Chimica Acta 2012, 390, 26. <http://dx.doi.org/10.1016/j.ica.2012.03.055>
• Pandiarajan Devaraj, Ramesh Rengan: Suzuki���Miyaura cross-coupling reaction of aryl bromides catalyzed by palladium(II) pyridoxal hydrazone complexes. Journal of Organometallic Chemistry 2012. <http://dx.doi.org/10.1016/j.jorganchem.2012.02.010>
• Xiao Huiping, Yu Lei, Li Yanhu, Yang Wen, Zhang Bin, Yang Wei, Wu Hongbin, Cao Yong: Novel green light-emitting polyfluorenes containing dibenzothiophene-S,S-dioxide-arylamine derivatives. Polymer 2012, 53, 2873. <http://dx.doi.org/10.1016/j.polymer.2012.05.011>
• Liu Mingjing, Ye Zhiqiang, Wang Guilan, Yuan Jingli: Synthesis and time-gated fluorometric application of a europium(III) complex with a borono-substituted terpyridine polyacid ligand. Talant 2012, 91, 116. <http://dx.doi.org/10.1016/j.talanta.2012.01.028>
• Karami Kazem, Rahimi Naser, Shehni Mahlagha Bahrami: Cyclopalladated complexes of 2-phenylaniline and their catalytic activity in Suzuki and Heck reactions under mild conditions. Tetrahedron Letters 2012, 53, 2428. <http://dx.doi.org/10.1016/j.tetlet.2012.03.003>
• Zhou Jing, Huang Liang-Zhu, Li You-Qiang, Du Zhen-Ting: Synthesis of substituted 6H-benzo[c]chromenes: a palladium promoted ring closure of diazonium tetrafluoroborates. Tetrahedron Letters 2012, 53, 7036. <http://dx.doi.org/10.1016/j.tetlet.2012.10.038>
• Zhao Shu-Chun, Ji Ke-Gong, Lu Lei, He Ting, Zhou An-Xi, Yan Ru-Long, Ali Shaukat, Liu Xue-Yuan,, Liang Yong-Min: Palladium-Catalyzed Divergent Reactions of 1,6-Enyne Carbonates: Synthesis of Vinylidenepyridines and Vinylidenepyrrolidines. J Org Chern 2012, 77, 2763. <http://dx.doi.org/10.1021/jo202590w>
• He Xiaoshuang, Zhang Shusheng, Guo Yinlong, Wang Haoyang, Lin Guoqiang: Mechanistic Investigations of a Palladium-Diene Catalyzed Suzuki–Miyaura Cross-Coupling Reaction. Organomettalics 2012, 31, 2945. <http://dx.doi.org/10.1021/om300115x>
• Rao Gyandshwar Kumar, Kumar Arun, Kumar Bharat, Kumar Dinesh, Singh Ajai Kumar: Palladium(ii)-selenated Schiff base complex catalyzed Suzuki–Miyaura coupling: Dependence of efficiency on alkyl chain length of ligand. DALTON T 2012, 41, 1931. <http://dx.doi.org/10.1039/c1dt11695a>
• Ma Heng-chang, Cao Wei, Bao Zhi-kang, Lei Zi-Qiang: Biopolymer–metal complex wool–Pd as a highly active catalyst for Suzuki reaction in water. Catal. Sci. Technol. 2012, 2, 2291. <http://dx.doi.org/10.1039/c2cy20126g>
• Merino Pedro, Tejero Tomas, Marca Eduardo, Gomollón-Bel Fernando, Delso Ignacio, Matute Rosa: CROSS-COUPLING REACTIONS FOR THE SYNTHESIS OF C-GLYCOSIDES AND RELATED COMPOUNDS. HETEROCYCLES 2012, 86, 791. <http://dx.doi.org/10.3987/REV-12-SR(N)3>
• Řezníček Tomáš, Dostál Libor, Růžička Aleš, Kulhánek Jiří, Bureš Filip, Jambor Roman: Palladium(II) complexes of Y,C,Y-chelated phosphines: synthesis, structure, and catalytic activity in Suzuki-Miyaura reaction. Appl Organometal Chem 2011, 25, 173. <http://dx.doi.org/10.1002/aoc.1737>
• Amatore Christian, Jutand Anny, Le Duc Gaëtan: Kinetic Data for the Transmetalation/Reductive Elimination in Palladium-Catalyzed Suzuki-Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as Base. Chem. Eur. J. 2011, 17, 2492. <http://dx.doi.org/10.1002/chem.201001911>
• Dey Somnath, Efimov Alexander, Lemmetyinen Helge: Bay Region Borylation of Perylene Bisimides. Eur J Org Chem 2011, 2011, 5955. <http://dx.doi.org/10.1002/ejoc.201101051>
• Schumacher Ricardo F., Rosário Alisson R., Souza Ana C.G., Acker Carmine I., Nogueira Cristina W., Zeni Gilson: The potential antioxidant activity of 2,3-dihydroselenophene, a prototype drug of 4-aryl-2,3-dihydroselenophenes. Bioorganic & Medicinal Chemistry 2011, 19, 1418. <http://dx.doi.org/10.1016/j.bmc.2011.01.005>
• Karami Kazem, Rizzoli Corrado, Salah Mina Mohamadi: Synthesis and application of ortho-palladated complex of (4-phenylbenzoylmethylene)triphenylphosphorane as a highly active catalyst in the Suzuki cross-coupling reaction. J Organomet Chem 2011, 696, 940. <http://dx.doi.org/10.1016/j.jorganchem.2010.10.025>
• Gladding Jeffery A., Bacci James P., Shaw Scott A., Smith Amos B.: Sporolide B: synthetic studies. Tetrahedron 2011, 67, 6697. <http://dx.doi.org/10.1016/j.tet.2011.04.094>
• Barbero Margherita, Bazzi Stefano, Cadamuro Silvano, Di Bari Lorenzo, Dughera Stefano, Ghigo Giovanni, Padula Daniele, Tabasso Silvia: Synthesis of 3-aryl-4-methyl-1,2-benzenedisulfonimides, new chiral Brønsted acids. A combined experimental and theoretical study. Tetrahedron 2011, 67, 5789. <http://dx.doi.org/10.1016/j.tet.2011.05.127>
• William Anthony D., Lee Angeline C.-H., Blanchard Stéphanie, Poulsen Anders, Teo Ee Ling, Nagaraj Harish, Tan Evelyn, Chen Dizhong, Williams Meredith, Sun Eric T.: Discovery of the Macrocycle 11-(2-Pyrrolidin-1-yl-ethoxy)-14,19-dioxa-5,7,26-triaza-tetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8,10,12(27),16,21,23-decaene (SB1518), a Potent Janus Kinase 2/Fms-Like Tyrosine Kinase-3 (JAK2/FLT3) Inhibitor for the Treatment of Myelofibrosis and Lymphoma. J Med Chem 2011, 54, 4638. <http://dx.doi.org/10.1021/jm200326p>
• Reginato Gloriana, Sadler Paul, Wilkes Robin D.: Scaling up Metal Scavenging Operations for Pharmaceutical Pilot Plant Manufactures. J Org Process Res Dev 2011, 15, 1396. <http://dx.doi.org/10.1021/op200127y>
• Cai Mingzhong, Peng Jian, Hao Wenyan, Ding Guodong: A phosphine-free carbonylative cross-coupling reaction of aryl iodides with arylboronic acids catalyzed by immobilization of palladium in MCM-41. Green Chem 2011, 13, 190. <http://dx.doi.org/10.1039/c0gc00138d>
• Nishida Mayumi, Tagata Tsuyoshi: Recent Progress in the Preparation of Organoboron Reagents via Direct Borylations. J Syn Org Chem Jpn 2011, 69, 1212. <http://dx.doi.org/10.5059/yukigoseikyokaishi.69.1212>
• Lü Bo, Fu Chunling, Ma Shengming: Application of Dicyclohexyl-(S )-trimethoxyphenyl Phosphine⋅HBF4 Salt for the Highly Selective Suzuki Coupling of the CCl Bond in β-Chlorobutenolides Over the More Reactive Allylic CO Bond. Chemistry - A European Journal 2010, 16, 6434. <http://dx.doi.org/10.1002/chem.201000169>
• Xie Xin-Gang, Wu Xun-Wei, Lee Hing-Ken, Peng Xiao-Shui, Wong Henry N. C.: Total Synthesis of Plakortone B. Chem Eur J 2010, 16, 6933. <http://dx.doi.org/10.1002/chem.201000189>
• SUZUKI A.: ChemInform Abstract: Synthetic Studies via the Cross-Coupling Reaction of Organoboron Derivatives with Organic Halides. ChemInform 2010, 22, no. <http://dx.doi.org/10.1002/chin.199123307>
• Ma Sheng-Ming, Shi Zhang-Jie: Synthesis of 4-halo-2 (5H)-furanones and their suzuki-coupling reactions with organoboronic acids. A general route to 4-aryl-2 (5 H) -furanones. Chin J Chem 2010, 19, 1280. <http://dx.doi.org/10.1002/cjoc.20010191220>
• Venkateshwarlu Gattu, Premalatha Akarapu, Chakradhar Anuganti, Rajanna Kamatala Chinna, Prakash Pondichery Kuppuswamy Sai: Peroxide/Potassium Iodide Redox Systems for in situ Oxyiodination of Organic Compounds under Liquid-Phase and Solvent-Free Conditions. HCA 2010, 93, 345. <http://dx.doi.org/10.1002/hlca.200900188>
• Revesz Laszlo, Schlapbach Achim, Aichholz Reiner, Dawson Janet, Feifel Roland, Hawtin Stuart, Littlewood-Evans Amanda, Koch Guido, Kroemer Markus, Möbitz Henrik, Scheufler Clemens, Velcicky Juraj, Huppertz Christine: In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part II. Bioorganic & Medicinal Chemistry Letters 2010, 20, 4719. <http://dx.doi.org/10.1016/j.bmcl.2010.04.023>
• Revesz Laszlo, Schlapbach Achim, Aichholz Reiner, Feifel Roland, Hawtin Stuart, Heng Richard, Hiestand Peter, Jahnke Wolfgang, Koch Guido, Kroemer Markus, Möbitz Henrik, Scheufler Clemens, Velcicky Juraj, Huppertz Christine: In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part I. Bioorganic & Medicinal Chemistry Letters 2010, 20, 4715. <http://dx.doi.org/10.1016/j.bmcl.2010.04.024>
• Li Tao, Bunnelle William H., Ryther Keith B., Anderson David J., Malysz John, Helfrich Rosalind, Grønlien Jens H., Håkerud Monika, Peters Dan, Schrimpf Michael R., Gopalakrishnan Murali, Ji Jianguo: Syntheses and structure–activity relationship (SAR) studies of 2,5-diazabicyclo[2.2.1]heptanes as novel α7 neuronal nicotinic receptor (NNR) ligands. Bioorganic & Medicinal Chemistry Letters 2010, 20, 3636. <http://dx.doi.org/10.1016/j.bmcl.2010.04.105>
• Chinelatto L.S., del Barrio J., Piñol M., Oriol L., Matranga M.A., De Santo M.P., Barberi R.: Oligofluorene blue emitters for cholesteric liquid crystal lasers. J Photochem Photobiol A Chem 2010, 210, 130. <http://dx.doi.org/10.1016/j.jphotochem.2010.01.006>
• Córdoba Marta, Castillo Rafael R., Izquierdo M. Luisa, Alvarez-Builla Julio: Pd-catalyzed reactions on pyridinium N-heteroarylaminides. Step-by-step synthesis of 3,5-unsymmetrically disubstituted 2-aminopyridines. Tetrahedron 2010, 66, 2624. <http://dx.doi.org/10.1016/j.tet.2010.02.036>
• Karnahl Michael, Tschierlei Stefanie, Kuhnt Christian, Dietzek Benjamin, Schmitt Michael, Popp Jürgen, Schwalbe Matthias, Krieck Sven, Görls Helmar, Heinemann Frank W.: Synthesis and characterization of regioselective substituted tetrapyridophenazine ligands and their Ru(ii) complexes. Dalton Trans 2010, 39, 2359. <http://dx.doi.org/10.1039/b917484b>
• Rao Gyandshwar Kumar, Kumar Arun, Ahmed Jahangeer, Singh Ajai Kumar: Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki–Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15. Chem Commun 2010, 46, 5954. <http://dx.doi.org/10.1039/c0cc01075h>
• Zhang Hui-jun, Wei Junnian, Zhao Fei, Liang Yun, Wang Zitao, Xi Zhenfeng: Selective synthesis of dibenzo[a,c]cyclooctatetraenes via palladium-catalyzed [4+4] cyclic homocoupling of borylvinyl iodobenzene derivatives. Chem Commun 2010, 46, 7439. <http://dx.doi.org/10.1039/c0cc02380a>
• Mao Jincheng, Hua Qiongqiong, Xie Guanlei, Guo Jun, Yao Zhigang, Shi Daqing, Ji Shunjun: Iodine-Catalyzed Suzuki-Miyaura Coupling Performed in Air. Adv Synth Catal 2009, 351, 635. <http://dx.doi.org/10.1002/adsc.200800624>
• Karnahl Michael, Krieck Sven, G��rls Helmar, Tschierlei Stefanie, Schmitt Michael, Popp J��rgen, Chartrand Daniel, Hanan Garry S., Groarke Robert, Vos Johannes G.: Synthesis and Photophysical Properties of 3,8-Disubstituted 1,10-Phenanthrolines and Their Ruthenium(II) Complexes. Eur J Inorg Chem 2009, 2009, 4962. <http://dx.doi.org/10.1002/ejic.200900310>
• Giroux Marc-André, Guérard Kimiaka C., Beaulieu Marc-André, Sabot Cyrille, Canesi Sylvain: Alternative Coupling Reaction with Unactivated Furan Derivatives. Eur J Org Chem 2009, 2009, 3871. <http://dx.doi.org/10.1002/ejoc.200900542>
• Hall Adrian, Brown Susan H., Budd Christopher, Clayton Nicholas M., Giblin Gerard M.P., Goldsmith Paul, Hayhow Thomas G., Hurst David N., Naylor Alan, Anthony Rawlings D.: Discovery of GSK345931A: An EP1 receptor antagonist with efficacy in preclinical models of inflammatory pain. Biorg Med Chem Lett 2009, 19, 497. <http://dx.doi.org/10.1016/j.bmcl.2008.11.032>
• Li Ming, Hua Ruimao: Gold(I)-catalyzed direct C–H arylation of pyrazine and pyridine with aryl bromides. Tetrahetron Lett 2009, 50, 1478. <http://dx.doi.org/10.1016/j.tetlet.2009.01.059>
• Das Bhaskar C., Mahalingam Sakkarapalayam M., Evans Todd, Kabalka George W., Anguiano J., Hema K.: Design and synthesis of (E)-1-((3-ethyl-2,4,4-trimethylcyclohex-2-enylidene)methyl-4-substituted benzenes from 1-(2,6,6-trimethylcyclohex-1-enyl)ethanol. Chem Commun 2009, 2133. <http://dx.doi.org/10.1039/b823063c>
• Zhou Hai, Chung Wan-Jun, Xu Yun-He, Loh Teck-Peng: Direct arylation of cyclic enamides via Pd(ii)-catalyzed C–H activation. Chem Commun 2009, 3472. <http://dx.doi.org/10.1039/b903151k>
• Moghaddam Firouz Matloubi, Zargarani Dordaneh: Regioselective Bromination of Aromatic Amines and Phenols Using N-Benzyl-DABCO Tribromide. Synth Comm 2009, 39, 4212. <http://dx.doi.org/10.1080/00397910902898569>
• Vinci Daniele, Martins Nelson, Saidi Ourida, Bacsa John, Brigas Amadeu, Xiao Jianliang: Ferrocenyl phosphine–oxazaphospholidine oxide ligands for the Suzuki–Miyaura coupling of hindered aryl bromides and chlorides. Can J Chem 2009, 87, 171. <http://dx.doi.org/10.1139/v08-113>
• Alonso Francisco, Beletskaya Irina P., Yus Miguel: Non-conventional methodologies for transition-metal catalysed carbon–carbon coupling: a critical overview. Part 2: The Suzuki reaction. Tetrahedron 2008, 64, 3047. <http://dx.doi.org/10.1016/j.tet.2007.12.036>
• Mao Jincheng, Guo Jun, Fang Fubing, Ji Shun-Jun: Highly efficient copper(0)-catalyzed Suzuki–Miyaura cross-coupling reactions in reusable PEG-400. Tetrahedron 2008, 64, 3905. <http://dx.doi.org/10.1016/j.tet.2008.02.068>
• Doan Ngoc-Duc, Bourgault Steve, Létourneau Myriam, Fournier Alain: Effectiveness of the Suzuki−Miyaura Cross-Coupling Reaction for Solid-Phase Peptide Modification. J. Comb. Chem. 2008, 10, 44. <http://dx.doi.org/10.1021/cc700128b>
• Servin Paul, Laurent Régis, Romerosa Antonio, Peruzzini Maurizio, Majoral Jean-Pierre, Caminade Anne-Marie: Synthesis of Dendrimers Terminated by Bis(diphenylphosphinomethyl)amino Ligands and Use of Their Palladium Complexes for Catalyzing C−C Cross-Coupling Reactions. Organometallics 2008, 27, 2066. <http://dx.doi.org/10.1021/om800008p>
• Sánchez-García David, Sessler Jonathan L.: Porphycenes: synthesis and derivatives. Chem Soc Rev 2008, 37, 215. <http://dx.doi.org/10.1039/b704945e>
• Niembro Sandra, Vallribera Adelina, Moreno-Mañas Marcial: Star-shaped heavily fluorinated aromatic sulfurs: stabilization of palladium nanoparticles active as catalysts in cross-coupling reactions. New J Chem 2008, 32, 94. <http://dx.doi.org/10.1039/b707776a>
• Shahid Muhammad, Imtiaz-ud-Din, Mazhar Muhammad, Zeller Matthias, Hunter Allen D.: [Bis(diphenylphosphino)methane-κ² P,P′]dichloridopalladium(II). Acta Crystallogr E Struct Rep Online 2008, 65, m158. <http://dx.doi.org/10.1107/S1600536808042980>
• Ma Ji, Cui Xiuling, Gao Liuyi, Wu Yangjie: Ferrocenylimidazoline palladacycles: Syntheses, crystal structures and applications as catalysts for Suzuki cross coupling reaction in water. J Inorg Chem Commun 2007, 10, 762. <http://dx.doi.org/10.1016/j.inoche.2007.03.018>
• Yadav Jhillu S., Gayathri Kamakolanu Uma, Ather Hissana, Rehman Hafeez ur, Prasad Attaluri R.: Utility of semicarbazones as ligands in newly made palladium complex for facile Suzuki homocoupling reaction of alkyl and aryl boronic acids. Journal of Molecular Catalysis A 2007, 271, 25. <http://dx.doi.org/10.1016/j.molcata.2007.01.012>
• Ma Ji, Cui Xiuling, Zhang Bi, Song Maoping, Wu Yangjie: Ferrocenylimidazoline palladacycles: efficient phosphine-free catalysts for Suzuki–Miyaura cross-coupling reaction. Tetrahedron 2007, 63, 5529. <http://dx.doi.org/10.1016/j.tet.2007.04.022>
• Jilani J. A.: A one-pot synthesis of 8-amino-1-methoxy-6H-dibenzo[b,d]pyran-6-one. Chem Pap 2007, 61, 410. <http://dx.doi.org/10.2478/s11696-007-0056-x>
• Ma Shengming, Jiang Xuefeng, Cheng Xin, Hou Hairong: Highly Efficient Suzuki Coupling Reaction of α-Chloroalkylidene-β-lactones and β-Lactams with Organoboronic Acids. Adv Synth Catal 2006, 348, 2114. <http://dx.doi.org/10.1002/adsc.200600234>
• Wang Jianhua, Fang Yuan-Qing, Bourget-Merle Laurence, Polson Matthew I. J., Hanan Garry S., Juris Alberto, Loiseau Frédérique, Campagna Sebastiano: The Multichromophore Approach: Prolonged Room-Temperature Luminescence Lifetimes in RuII Complexes Based on Tridentate Polypyridine Ligands. Chem Eur J 2006, 12, 8539. <http://dx.doi.org/10.1002/chem.200600245>
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