Pure and Applied Chemistry

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• Ye Bin, Wang Lin, Hu Xinquan, Redshaw Carl, Sun Wen-Hua: 2-(1-Aryliminoethyl)cycloheptapyridylpalladium complexes: Synthesis, characterization and the use in the Heck-reaction. Inorganica Chimica Acta 2013, 407, 281. <http://dx.doi.org/10.1016/j.ica.2013.08.008>
• Bagherzadeh Mojtaba, Amini Mojtaba, Ellern Arkady, Keith Woo L.: Palladium and copper complexes with oxygen–nitrogen mixed donors as efficient catalysts for the Heck reaction. Inorg Chim Ada 2012, 383, 46. <http://dx.doi.org/10.1016/j.ica.2011.10.040>
• Cuenú Fernando, Abonia Rodrigo, Bolaños Alberto, Cabrera Armando: Synthesis, structural elucidation and catalytic activity toward a model Mizoroki–Heck C–C coupling reaction of the pyrazolic Tröger’s base Pd4Cl8(PzTB)2 complex. Journal of Organometallic Chemistry 2011, 696, 1834. <http://dx.doi.org/10.1016/j.jorganchem.2011.02.016>
• Koutentis Panayiotis A., Loizou Georgia, Lo Re Daniele: Synthesis of Triazafluoranthenones via Silver(I)-Mediated Nonoxidative and Oxidative Intramolecular Palladium-Catalyzed Cyclizations. J Org Chern 2011, 76, 5793. <http://dx.doi.org/10.1021/jo200966k>
• Yu Xiao-Jun, Zhou Rong, Zhang Yu, Fu Hai-Yan, Li Rui-Xiang, Chen Hua, Li Xian-Jun: Heck coupling reaction catalyzed by [(C3H5)PdCl]2-N,N,N′,N′-tetra(diphenylphosphinomethyl)-1,2-ethylenediamine. Catal Commun 2010, 12, 222. <http://dx.doi.org/10.1016/j.catcom.2010.07.007>
• Burns Michael J., Thatcher Robert J., Taylor Richard J. K., Fairlamb Ian J. S.: Pd-catalysed regioselective C–H functionalisation of 2-pyrones. Dalton Trans 2010, 39, 10391. <http://dx.doi.org/10.1039/c0dt00421a>
• Phan Nam T. S., Van Der Sluys Matthew, Jones Christopher W.: On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review. Adv Synth Catal 2006, 348, 609. <http://dx.doi.org/10.1002/adsc.200505473>
• Naidu B. Vijaya Kumar, Jin Sung-Ho, Kim Sung-Chul, Shin Won-Suk, Lee Jae Wook, Gal Yeong-Soon: Effect of desilylation on the optical and electroluminescence properties of poly[2-(3-dimethyldodecylsilylphenyl)-1,4-phenylenevinylene]. J Polym Sci A Polym Chem 2006, 44, 6498. <http://dx.doi.org/10.1002/pola.21734>
• Prukała Wiesław, Majchrzak Mariusz, Pietraszuk Cezary, Marciniec Bogdan: Highly stereoselective synthesis of E-4-chlorostilbene and its derivatives via tandem cross-metathesis (or silylative coupling) and Hiyama coupling. Journal of Molecular Catalysis A 2006, 254, 58. <http://dx.doi.org/10.1016/j.molcata.2006.03.027>
• Cai Mingzhong, Tong Xiaokai, Hu Wenying, Huang Yizheng: Silica-bound poly-4-oxa-6,7-bis(diphenylarsino)heptylsiloxane palladium(0) complex catalyzed Heck arylation of butyl acrylate and acrylamide with aryl halides. React & Funct Polym 2006, 66, 531. <http://dx.doi.org/10.1016/j.reactfunctpolym.2005.10.006>
• Ming-Zhong Cai, Hong Zhao, Wen-Ying Hu: Silica-Supported Arsine Palladium(0) Complex: a Highly Active and Stereoselective Catalyst for Arylation of Butyl Acrylate and Acrylamide. Chin J Chem 2005, 23, 443. <http://dx.doi.org/10.1002/cjoc.200590443>
• Cai Mingzhong, Liu Gang, Zhou Jun: Synthesis of silica-supported poly-ω-(methylseleno)undecylsiloxane palladium(0) complex and its catalytic properties for Heck arylation of alkenes. Journal of Molecular Catalysis A 2005, 227, 107. <http://dx.doi.org/10.1016/j.molcata.2004.10.015>
• Yang Hengquan, Zhang Gaoyong, Hong Xinlin, Zhu Yinyan: Dicyano-functionalized MCM-41 anchored-palladium complexes as recoverable catalysts for Heck reaction. Journal of Molecular Catalysis A 2004, 210, 143. <http://dx.doi.org/10.1016/j.molcata.2003.09.009>
• Cai Mingzhong, Huang Yizheng, Zhao Hong, Song Caisheng: Synthesis of silica-supported poly-γ-diphenylarsinopropylsiloxane palladium(0) complex and its catalytic properties for Heck arylation of conjugated alkenes. React & Funct Polym 2004, 59, 81. <http://dx.doi.org/10.1016/j.reactfunctpolym.2003.12.009>
• Tsai Fu-Yu, Wu Chen-Lin, Mou Chung-Yuan, Chao Man-Chien, Lin Hong-Ping, Liu Shiuh-Tzung: Palladium bipyridyl complex anchored on nanosized MCM-41 as a highly efficient and recyclable catalyst for Heck reaction. Tetrahetron Lett 2004, 45, 7503. <http://dx.doi.org/10.1016/j.tetlet.2004.08.065>
• Cai Mingzhong, Huang Yizheng, Zhao Hong, Song Caisheng: Silica-supported bidentate arsine palladium(0) complex: a highly active and stereoselective catalyst for arylation of conjugated alkenes. J Organomet Chem 2003, 682, 20. <http://dx.doi.org/10.1016/S0022-328X(03)00668-5>
• Zhou Jianmin, Zhou Renxian, Mo Liuye, Zhao Shaofen, Zheng Xiaoming: MCM-41 supported aminopropylsiloxane palladium(0) complex: a highly active and stereoselective catalyst for Heck reaction. Journal of Molecular Catalysis A 2002, 178, 289. <http://dx.doi.org/10.1016/S1381-1169(01)00245-X>
• de Meijere Armin, Zhong Song Zhi, Lansky Annegret, Hyuda Syed, Rauch Karsten, Noltemeyer Mathias, König Burkhard, Knieriem Burkhard: Palladium-Catalyzed Self-Cross Coupling ofo-Bromo-trans-stilbenes To Yield 9,10-Bis(arylmethylene)-9,10-dihydroanthracenes©. Eur J Org Chem 1998, 1998, 2289. <http://dx.doi.org/10.1002/(SICI)1099-0690(199811)1998:11<2289::AID-EJOC2289>3.0.CO;2-Z>
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• Bykov V. V., Bumagin N. A.: Effect of water on the palladium-catalyzed reaction of styrene with iodobenzene. Russ Chem Bull 1997, 46, 1346. <http://dx.doi.org/10.1007/BF02495940>
• Wang Qian, Liu Hanfan, Han Ming, Li Xiaobao, Jiang Dazhi: Carbonylation of methanol catalyzed by polymer-protected rhodium colloid. Journal of Molecular Catalysis A 1997, 118, 145. <http://dx.doi.org/10.1016/S1381-1169(96)00387-1>
• Villar Lourdes, Bullock Joseph P., Khan Matheen M., Nagarajan Arumugam, Bates Roderick W., Bott Simon G., Zepeda Gerardo, Delgado Francisco, Tamariz Joaquin: Highly stereoselective palladium-catalyzed coupling reactions of captodative olefins acetylvinyl arenecarboxylates. J Organomet Chem 1996, 517, 9. <http://dx.doi.org/10.1016/0022-328X(96)06112-8>
• Bumagin N.A., Bykov V.V., Sukhomlinova L.I., Tolstaya T.P., Beletskaya I.P.: Palladium-catalyzed arylation of styrene and acrylic acid in water. J Organomet Chem 1995, 486, 259. <http://dx.doi.org/10.1016/0022-328X(94)05056-H>
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