Pure and Applied Chemistry

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• Mąkosza Mieczysław: Reactions of Nucleophiles with Nitroarenes: Multifacial and Versatile Electrophiles. Chem. Eur. J. 2014, n/a. <http://dx.doi.org/10.1002/chem.201400097>
• Abourahma Heba, Bradley Lynn, Lareau Nichole M., Reesbeck Megan: Modified Birch Reduction for the Introductory Undergraduate Organic Laboratory. J. Chem. Educ. 2014, 91, 443. <http://dx.doi.org/10.1021/ed4000537>
• Kim Ye Ji, Kim Sun Min, Hosono Hideo, Yang Jung Woon, Kim Sung Wng: The scalable pinacol coupling reaction utilizing the inorganic electride [Ca2N]+·e− as an electron donor. Chem. Commun. 2014, 50, 4791. <http://dx.doi.org/10.1039/c4cc00802b>
• Ren Ying, Jia Jianfeng, Zhang Ting-Ting, Wu Hai-Shun, Liu Wenxian: Computational Study on the Palladium-Catalyzed Allenylative Dearomatization Reaction. Organomettalics 2012, 31, 1168. <http://dx.doi.org/10.1021/om201248t>
• Donohoe Timothy J., Pullin Robert D. C.: Natural product synthesis as a challenging test of newly developed methodology. Chem. Commun. 2012, 48, 11924. <http://dx.doi.org/10.1039/c2cc36040c>
• Segawa Yasutomo, Stephan Douglas W.: Metal-free hydrogenation catalysis of polycyclic aromatic hydrocarbons. Chem. Commun. 2012, 48, 11963. <http://dx.doi.org/10.1039/c2cc37190a>
• Ji Pengju, Atherton John, Page Michael I.: Organic reactivity in liquid ammonia. Org. Biomol. Chem. 2012, 10, 5732. <http://dx.doi.org/10.1039/c2ob25064k>
• Lee Sunyoung, Chataigner Isabelle, Piettre Serge R.: Facile Dearomatization of Nitrobenzene Derivatives and Other Nitroarenes with N-Benzyl Azomethine Ylide. Angew Chem 2011, 123, 492. <http://dx.doi.org/10.1002/ange.201005779>
• Lee Sunyoung, Chataigner Isabelle, Piettre Serge R.: Facile Dearomatization of Nitrobenzene Derivatives and Other Nitroarenes with N-Benzyl Azomethine Ylide. Angew Chem Int Ed 2011, 50, 472. <http://dx.doi.org/10.1002/anie.201005779>
• Donald Kelling J., Bober Matthew: Predicting the Relative Stability of Simple versus ansa-Sandwich Systems Across Groups: Structure, Bonding, and (In)Stability in Tris(sandwich)benzene Complexes. Chem Eur J 2011, 17, 1936. <http://dx.doi.org/10.1002/chem.201001381>
• Paptchikhine Alexander, Itto Kaori, Andersson Pher G.: Sequential Birch reaction and asymmetric Ir-catalyzed hydrogenation as a route to chiral building blocks. Chem Commun 2011, 47, 3989. <http://dx.doi.org/10.1039/c0cc05619g>
• BIRCH A. J.: ChemInform Abstract: The Birch Reduction in Organic Synthesis. ChemInform 2010, 27, no. <http://dx.doi.org/10.1002/chin.199643264>
• Nador Fabiana, Moglie Yanina, Vitale Cristian, Yus Miguel, Alonso Francisco, Radivoy Gabriel: Reduction of polycyclic aromatic hydrocarbons promoted by cobalt or manganese nanoparticles. Tetrahedron 2010, 66, 4318. <http://dx.doi.org/10.1016/j.tet.2010.04.026>
• Ji Pengju, Atherton John H., Page Michael I.: The kinetics and mechanisms of organic reactions in liquid ammonia. Faraday Disc 2010, 145, 15. <http://dx.doi.org/10.1039/b912261n>
• Bulbrook Michelle, Chu Minghui, Deane Karen, Doyle Roy J., Hinc Justina, Peterson Charlotte, Salem Geoffrey, Thorman Nadia, Willis Anthony C.: Chiral Birch reduced tertiary phosphines: precursors to asymmetric 1,2-cyclohexenebis(tertiary phosphines). Dalton Trans 2010, 39, 8878. <http://dx.doi.org/10.1039/c0dt00648c>
• Nicolaou K. C., Chen Jason S., Edmonds David J., Estrada Anthony A.: Fortschritte in der Chemie und Biologie natürlicher Antibiotika. Angew Chem 2009, 121, 670. <http://dx.doi.org/10.1002/ange.200801695>
• Nicolaou K. C., Chen Jason S., Edmonds David J., Estrada Anthony A.: Recent Advances in the Chemistry and Biology of Naturally Occurring Antibiotics. Angew Chem Int Ed 2009, 48, 660. <http://dx.doi.org/10.1002/anie.200801695>
• Costanzo Michael J., Patel Mitul N., Petersen Kathryn A., Vogt Paul F.: Ammonia-free Birch reductions with sodium stabilized in silica gel, Na–SG(I). Tetrahetron Lett 2009, 50, 5463. <http://dx.doi.org/10.1016/j.tetlet.2009.07.040>
• Li Fuying, Yin Chenlei, Chen Jie, Liu Jinggen, Xie Xin, Zhang Ao: Synthesis and SAR Study of Opioid Receptor Ligands: Mono- and Bis-Indolomorphinans. Chem Biol Drug Design 2009, 74, 335. <http://dx.doi.org/10.1111/j.1747-0285.2009.00849.x>
• Lu Shirong, Xu Zhanwei, Bao Ming, Yamamoto Yoshinori: Carbocycle Synthesis through Facile and Efficient Palladium-Catalyzed Allylative De-aromatization of Naphthalene and Phenanthrene Allyl Chlorides. Angew Chem 2008, 120, 4438. <http://dx.doi.org/10.1002/ange.200800529>
• Lu Shirong, Xu Zhanwei, Bao Ming, Yamamoto Yoshinori: Carbocycle Synthesis through Facile and Efficient Palladium-Catalyzed Allylative De-aromatization of Naphthalene and Phenanthrene Allyl Chlorides. Angew Chem Int Ed 2008, 47, 4366. <http://dx.doi.org/10.1002/anie.200800529>
• Weber Immo, Heinemann Frank W., Bakatselos Panagiotis, Zenneck Ulrich: Stille Cross-Coupling of a Racemic Planar-Chiral Ferrocene and Crystallographic Trace Analysis of Catalysis Intermediates and By-products. HCA 2007, 90, 834. <http://dx.doi.org/10.1002/hlca.200790083>
• Bongat Aileen F.G., Demchenko Alexei V.: Recent trends in the synthesis of O-glycosides of 2-amino-2-deoxysugars. Carbohydrates Research 2007, 342, 374. <http://dx.doi.org/10.1016/j.carres.2006.10.021>
• Kukula Pavel, Dutly Andreas, Rüegger Heinz, Prins Roel: Molecular rearrangement in the Birch reduction of dibenzothiophenes. Tetrahetron Lett 2007, 48, 5657. <http://dx.doi.org/10.1016/j.tetlet.2007.06.026>
• Fan Gao-jun, Wang Zhongyi, Wee Andrew G. H.: Regio- and diastereocontrolled C?H insertion of chiral ?- and ?-lactam diazoacetates. Application to the asymmetric synthesis of (8S,8aS)-8-hydroxyindolizidine. Chem Commun 2006, 3732. <http://dx.doi.org/10.1039/b606436a>
• Mendoza Oscar, Müller-Bunz Helge, Tacke Matthias: Cocondensation reactions of nitrogen-containing heterocycles with lithium atoms at 77K. J Organomet Chem 2005, 690, 3357. <http://dx.doi.org/10.1016/j.jorganchem.2005.04.017>
• Hölemann Alexandra, Reißig Hans-Ulrich: Regioselective Samarium Diiodide Induced Couplings of Carbonyl Compounds with 1,3-Diphenylallene and Alkoxyallenes: A New Route to 4-Hydroxy-1-enol Ethers. Chem Eur J 2004, 10, 5493. <http://dx.doi.org/10.1002/chem.200400418>
• Labadie Guillermo R., Esti�� Guillermina L., Cravero Raquel M., Sierra Manuel Gonzalez, Hemmateenejad Bahram, Safarpour Mohammad A., Taghavi Fariba, Liu Xiao-Juan, Feng Ji-Kang, Ren Ai-Min, Zhou Xin: Decomposition mechanism of Birch alkylation products of ��-tetralones. Journal of Molecular Structure: THEOCHEM 2003, 635, 173. <http://dx.doi.org/10.1016/S0166-1280(03)00407-X>
• Smith Philip L., Chordia Mahendra D., Dean Harman W.: Synthetic applications of the dearomatization agent pentaammineosmium(II). Tetrahedron 2001, 57, 8203. <http://dx.doi.org/10.1016/S0040-4020(01)00805-5>
• Labadie Guillermo R., Cravero Raquel M., Gonzalez-Sierra Manuel: Studies of Birch Reductive Alkylation of Substituted α-Tetralones. Synth Common 2000, 30, 4065. <http://dx.doi.org/10.1080/00397910008087022>
• Radivoy Gabriel, Alonso Francisco, Yus Miguel: Reduction of sulfonates and aromatic compounds with the NiCl2·2H2OLi-arene (cat.) combination. Tetrahedron 1999, 55, 14479. <http://dx.doi.org/10.1016/S0040-4020(99)00893-5>
• Alonso Emma, Ramón Diego J., Yus Miguel: Naphthalene-catalysed lithiation of N,N-diisopropylbenzamide and its methoxy derivatives. Tetrahedron 1998, 54, 13629. <http://dx.doi.org/10.1016/S0040-4020(98)00839-4>
• Quayle P.: Chapter 4. Aliphatic and alicyclic chemistry. Annu Rep Prog Chem Sect B 1997, 93, 69. <http://dx.doi.org/10.1039/oc093069>