Pure and Applied Chemistry

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• Park Sae Hume, Kwak Jaesung, Shin Kwangmin, Ryu Jaeyune, Park Yoonsu, Chang Sukbok: Mechanistic Studies of the Rhodium-Catalyzed Direct C–H Amination Reaction Using Azides as the Nitrogen Source. J. Am. Chem. Soc. 2014, 136, 2492. <http://dx.doi.org/10.1021/ja411072a>
• Shin Kwangmin, Ryu Jaeyune, Chang Sukbok: Orthogonal Reactivity of Acyl Azides in C–H Activation: Dichotomy between C–C and C–N Amidations Based on Catalyst Systems. Org. Lett. 2014, 16, 2022. <http://dx.doi.org/10.1021/ol500602b>
• Budruev A. V., Sinjagina D. Yu.: Reactions of acyl azides with secondary amines in the presence of copper(ii) acetate. Russ Chem Bull 2013, 62, 1366. <http://dx.doi.org/10.1007/s11172-013-0194-y>
• Dequirez Geoffroy, Pons Valérie, Dauban Philippe: Nitren-Chemie in der organischen Synthese: noch in den Kinderschuhen?. Angew. Chem. 2012, 124, 7498. <http://dx.doi.org/10.1002/ange.201201945>
• Dequirez Geoffroy, Pons Valérie, Dauban Philippe: Nitrene Chemistry in Organic Synthesis: Still in Its Infancy?. Angew. Chem. Int. Ed. 2012, 51, 7384. <http://dx.doi.org/10.1002/anie.201201945>
• Kang Xiongwu, Song Yang, Chen Shaowei: Nitrene-functionalized ruthenium nanoparticles. J. Mater. Chem. 2012, 22, 19250. <http://dx.doi.org/10.1039/c2jm33783e>
• Zhang Yan, Feng Bainian, Zhu Chengjian: Au(iii)-catalyzed intermolecular amidation of benzylic C–H bonds. Org. Biomol. Chem. 2012, 10, 9137. <http://dx.doi.org/10.1039/c2ob26857d>
• Grigg R. David, Schomaker Jennifer M., Timokhin Vitaliy: C–H amination/cyclocarbonylation of allene carbamates: a versatile platform for the synthesis of α,β-unsaturated γ-lactams. Tetrahedron 2011, 67, 4318. <http://dx.doi.org/10.1016/j.tet.2011.03.026>
• Ton Thi My Uyen, Tejo Ciputra, Tania Stefani, Chang Joyce Wei Wei, Chan Philip Wai Hong: Iron(II)-Catalyzed Amidation of Aldehydes with Iminoiodinanes at Room Temperature and under Microwave-Assisted Conditions. J Org Chem 2011, 76, 4894. <http://dx.doi.org/10.1021/jo200284a>
• Lu Hongjian, Jiang Huiling, Wojtas Lukasz, Zhang X. Peter: Selective Intramolecular CH Amination through the Metalloradical Activation of Azides: Synthesis of 1,3-Diamines under Neutral and Nonoxidative Conditions. angew chemie 2010, 122, 10390. <http://dx.doi.org/10.1002/ange.201005552>
• Lu Hongjian, Jiang Huiling, Wojtas Lukasz, Zhang X. Peter: Selective Intramolecular CH Amination through the Metalloradical Activation of Azides: Synthesis of 1,3-Diamines under Neutral and Nonoxidative Conditions. Angew Chem Int Ed 2010, 49, 10192. <http://dx.doi.org/10.1002/anie.201005552>
• Leathen Matthew L., Peterson Emily A.: Facile preparation of protected benzylic and heteroarylmethyl amines via room temperature Curtius rearrangement. Tetrahetron Lett 2010, 51, 2888. <http://dx.doi.org/10.1016/j.tetlet.2010.03.101>
• Chang Joyce Wei Wei, Ton Thi My Uyen, Tania Stefani, Taylor Paul C., Chan Philip Wai Hong: Practical copper(i)-catalysed amidation of aldehydes. Chem Commun 2010, 46, 922. <http://dx.doi.org/10.1039/b918588g>
• Lebel Hélène, Parmentier Michaël: Copper-catalyzed enantioselective aziridination of styrenes. Pure and App Chemis 2010, 1. <http://dx.doi.org/10.1351/PAC-CON-09-12-12>
• Kurokawa Toshiki, Kim Mihyong, Du Bois J.: Synthesis of 1,3-Diamines Through Rhodium-Catalyzed CH Insertion. Angew. Chem. 2009, 121, 2815. <http://dx.doi.org/10.1002/ange.200806192>
• Kurokawa Toshiki, Kim Mihyong, Du Bois J.: Synthesis of 1,3-Diamines Through Rhodium-Catalyzed CH Insertion. Angew. Chem. Int. Ed. 2009, 48, 2777. <http://dx.doi.org/10.1002/anie.200806192>
• Fiori Kristin Williams, Espino Christine G., Brodsky Benjamin H., Du Bois J.: A mechanistic analysis of the Rh-catalyzed intramolecular C–H amination reaction. Tetrahedron 2009, 65, 3042. <http://dx.doi.org/10.1016/j.tet.2008.11.073>
• Fantauzzi Simone, Gallo Emma, Caselli Alessandro, Ragaini Fabio, Casati Nicola, Macchi Piero, Cenini Sergio: The key intermediate in the amination of saturated C–H bonds: synthesis, X-ray characterization and catalytic activity of Ru(TPP)(NAr)2 (Ar = 3,5-(CF3)2C6H3). Chem Commun 2009, 3952. <http://dx.doi.org/10.1039/b903238j>
• Leogane Olivier, Lebel Hélène: One-Pot Multicomponent Synthesis of Indoles from 2-Iodobenzoic Acid. Angew Chem 2008, 120, 356. <http://dx.doi.org/10.1002/ange.200703671>
• Leogane Olivier, Lebel Hélène: One-Pot Multicomponent Synthesis of Indoles from 2-Iodobenzoic Acid. Angew Chem Int Ed 2008, 47, 350. <http://dx.doi.org/10.1002/anie.200703671>
• Huard Kim, Lebel Hélène: N‐Tosyloxycarbamates as Reagents in Rhodium‐Catalyzed CH Amination Reactions. Chem Eur J 2008, 14, 6222. <http://dx.doi.org/10.1002/chem.200702027>
• Schröder Detlef, Schwarz Helmut, Aliaga-Alcalde Núria, Neese Frank: Fragmentation of the (Cyclam-acetato)iron Azide Cation in the Gas Phase. Eur J Inorg Chem 2007, 2007, 816. <http://dx.doi.org/10.1002/ejic.200600805>
• Klotz Katie L., Slominski Luke M., Hull Anthony V., Gottsacker Victoria M., Mas-Ballest? Rub?n, Que, Jr. Lawrence, Halfen Jason A.: Non-heme iron(ii) complexes are efficient olefin aziridination catalysts. Chem Commun 2007, 2063. <http://dx.doi.org/10.1039/b700493a>
• Harden Jeremiah D., Ruppel Joshua V., Gao Guang-Yao, Zhang X. Peter: Cobalt-catalyzed intermolecular C–H amination with bromamine-T as nitrene source. Chem Commun 2007, 4644. <http://dx.doi.org/10.1039/b710677g>
• Lebel Helen, Leogane Olivier, Huard Kim, Lectard Sylvain: Catalytic Activation of Nitrogen Derivatives with Transition-Metal Complexes. ChemInform 2006, 37. <http://dx.doi.org/10.1002/chin.200631254>
• Guthikonda Kiran, Wehn Paul M., Caliando Brian J., Du Bois J.: Rh-catalyzed alkene oxidation: a highly efficient and selective process for preparing N-alkoxysulfonyl aziridines. Tetrahedron 2006, 62, 11331. <http://dx.doi.org/10.1016/j.tet.2006.07.099>