Pure and Applied Chemistry

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• Koch Eva, Studer Armido: Regioselektive dreifache aromatische Substitution von Benzoesäurederivaten durch Dearomatisierung, regioselektive Funktionalisierung und Rearomatisierung. Angew. Chem. 2013, 125, 5033. <http://dx.doi.org/10.1002/ange.201300259>
• Koch Eva, Studer Armido: Regioselective Threefold Aromatic Substitution of Benzoic Acid Derivatives by Dearomatization, Regioselective Functionalization, and Rearomatization. Angew. Chem. Int. Ed. 2013, 52, 4933. <http://dx.doi.org/10.1002/anie.201300259>
• Meng Wen-Ting, Zheng Yan, Nie Jing, Xiong Heng-Ying, Ma Jun-An: Organocatalytic Asymmetric One-Pot Sequential Conjugate Addition/Dearomative Fluorination: Synthesis of Chiral Fluorinated Isoxazol-5(4H)-ones. J. Org. Chem. 2013, 78, 559. <http://dx.doi.org/10.1021/jo302419e>
• Cadu Alban, Andersson Pher G.: Iridium catalysis: application of asymmetric reductive hydrogenation. Dalton Trans. 2013, 42, 14345. <http://dx.doi.org/10.1039/c3dt51163d>
• Li Feng, Sun Long, Teng Yuou, Yu Peng, Zhao John Cong-Gui, Ma Jun-An: Highly Diastereo- and Enantioselective Organocatalytic One-Pot Sequential 1,4-Addition/Dearomative-Fluorination Transformation. Chem. Eur. J. 2012, 18, 14255. <http://dx.doi.org/10.1002/chem.201202636>
• Kinbara Atsushi, Yamagishi Takehiro, Hanzawa Naoko, Kawashima Etsuko, Miyaoka Hiroaki: Synthesis of Phenol Derivatives from Cyclohex-2-enones Bearing an Alkyne through Lewis Acid-Catalyzed Enolization and Intramolecular Alder–Rickert Reaction. J. Org. Chem. 2012, 77, 8999. <http://dx.doi.org/10.1021/jo301554z>
• Wu Ke-Jia, Dai Li-Xin, You Shu-Li: Palladium(0)-Catalyzed Dearomative Arylation of Indoles: Convenient Access to Spiroindolenine Derivatives. Org. Lett. 2012, 14, 3772. <http://dx.doi.org/10.1021/ol301663h>
• 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>
• 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>
• Chou Chih-Ming, Chatterjee Indranil, Studer Armido: Stereospecific Palladium-Catalyzed Decarboxylative C(sp3)C(sp2) Coupling of 2,5-Cyclohexadiene-1-carboxylic Acid Derivatives with Aryl Iodides. Angew Chem Int E 2011, 50, 8614. <http://dx.doi.org/10.1002/anie.201103450>
• Ibanez Jorge G., Guerra-Millan Francisco J., Hugerat Muhamad, Vazquez-Olavarrieta Jorge L., Basheer Ahmad, Abu-Much Riam: Readily Made Solvated Electrons. J Chem Ed 2011, 88, 670. <http://dx.doi.org/10.1021/ed100179d>
• 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>
• You Hai Tao, Grosse Andrew C., Howard James K., Hyland Christopher J. T., Just Jeremy, Molesworth Peter P., Smith Jason A.: Chemoselective reduction of 2-acyl-N-sulfonylpyrroles: Synthesis of 3-pyrrolines and 2-alkylpyrroles. Org Biomol Chem 2011, 9, 3948. <http://dx.doi.org/10.1039/c1ob05111c>
• Bramborg Andrea, Linker Torsten: Selective Synthesis of 1,4-Dialkylbenzenes from Terephthalic Acid. Synth Catal 2010, 352, 2195. <http://dx.doi.org/10.1002/adsc.201000322>
• Wang Sunewang R., Qiu Zaozao, Xie Zuowei: Insertion of Carboryne into Aromatic Rings: Formation of Cyclooctatetraenocarboranes. J Am Chem Soc 2010, 132, 9988. <http://dx.doi.org/10.1021/ja1044488>
• Krüger Tobias, Vorndran Katja, Linker Torsten: Regioselective Arene Functionalization: Simple Substitution of Carboxylate by Alkyl Groups. Chem Eur J 2009, 15, 12082. <http://dx.doi.org/10.1002/chem.200901774>
• 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>
• García-Fortanet Jorge, Kessler Florian, Buchwald Stephen L.: Palladium-Catalyzed Asymmetric Dearomatization of Naphthalene Derivatives. J Am Chem Soc 2009, 131, 6676. <http://dx.doi.org/10.1021/ja9025193>
• 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>
• Subba Rao G. S. R.: Birch Reduction and Its Application in the Total Synthesis of Natural Products. ChemInform 2004, 35. <http://dx.doi.org/10.1002/chin.200410264>