Pure and Applied Chemistry

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• Llaveria Josep, Beltrán Álvaro, Sameera W. M. C., Locati Abel, Díaz-Requejo M. Mar, Matheu M. Isabel, Castillón Sergio, Maseras Feliu, Pérez Pedro J.: Chemo-, Regio-, and Stereoselective Silver-Catalyzed Aziridination of Dienes: Scope, Mechanistic Studies, and Ring-Opening Reactions. J. Am. Chem. Soc. 2014, 136, 5342. <http://dx.doi.org/10.1021/ja412547r>
• Salomone Antonio, Perna Filippo M., Falcicchio Aurelia, Nilsson Lill Sten O., Moliterni Anna, Michel Reent, Florio Saverio, Stalke Dietmar, Capriati Vito: Direct observation of a lithiated oxirane: a synergistic study using spectroscopic, crystallographic, and theoretical methods on the structure and stereodynamics of lithiated ortho-trifluoromethyl styrene oxide. Chem. Sci. 2014, 5, 528. <http://dx.doi.org/10.1039/c3sc52099d>
• Aresu Emanuele, Carroccia Laura, Fioravanti Stefania, Pellacani Lucio: Desymmetrization of α-diimines: synthesis of new 3-(diaziridin-3-yl)oxaziridines. Tetrahedron Letters 2013, 54, 4574. <http://dx.doi.org/10.1016/j.tetlet.2013.06.090>
• Hughes Matthew, Boultwood Tom, Zeppetelli Gianfranco, Bull James A.: Palladium-Catalyzed Cross-Coupling of Aziridinylmetal Species, Generated by Sulfinyl–Magnesium Exchange, with Aryl Bromides: Reaction Optimization, Scope, and Kinetic Investigations. J. Org. Chem. 2013, 78, 844. <http://dx.doi.org/10.1021/jo3027824>
• Naeimi Hossein, Rabiei Khadijeh: A Novel Catalyst-Free One-Pot Synthesis of Some New N-(α-Hydroxybenzyl)formamides by Treatment of 2,2-Dichloroaziridines with Dimethyl Sulfoxide and Water under Neutral Conditions. HCA 2012, 95, 1102. <http://dx.doi.org/10.1002/hlca.201100453>
• Lebel Hélène, Parmentier Michaël, Leogane Olivier, Ross Karen, Spitz Cédric: Copper bis(oxazolines) as catalysts for stereoselective aziridination of styrenes with N-tosyloxycarbamates. Tetrahedron 2012, 68, 3396. <http://dx.doi.org/10.1016/j.tet.2012.02.044>
• Pratt Lawrence M., Mai Binh Khanh, Ramachandran B. Ramu: Carbenoid Alkene Insertion Reactions of Oxiranyllithiums. J. Org. Chem. 2012, 77, 8605. <http://dx.doi.org/10.1021/jo301550y>
• Bull James A., Boultwood Tom, Taylor Thomas A.: Highly cis-selective synthesis of iodo-aziridines using diiodomethyllithium and in situ generated N-Boc-imines. Chem. Commun. 2012, 48, 12246. <http://dx.doi.org/10.1039/c2cc37029h>
• M. Hodgson David, A. H. Stent Matthew, S. Paton Robert, X. Wilson Francis: Unusual Base-Induced Rearrangement of exo-9-Oxabicyclo[4.2.1]non-7-ene Oxide to exo-8-Hydroxybicyclo[3.3.0]octan-2-one. Heterocycle 2012, 84, 625. <http://dx.doi.org/10.3987/COM-11-S(P)35>
• Yoshida Jun-ichi, Kim Heejin, Nagaki Aiichiro: Green and Sustainable Chemical Synthesis Using Flow Microreactors. ChemSusChem 2011, 4, 331. <http://dx.doi.org/10.1002/cssc.201000271>
• Tsarevsky Nicolay V., Jakubowski Wojciech: Atom transfer radical polymerization of functional monomers employing Cu-based catalysts at low concentration: Polymerization of glycidyl methacrylate. J Polym Sci A Polym Chem 2011, 49, 918. <http://dx.doi.org/10.1002/pola.24503>
• Roe Caroline, Solá Toni Moragas, Sasraku-Neequaye Leonid, Hobbs Heather, Churcher Ian, MacPherson David, Stockman Robert A.: On the utility of S-mesitylsulfinimines for the stereoselective synthesis of chiral amines and aziridines. Chem Commun 2011, 47, 7491. <http://dx.doi.org/10.1039/c1cc11870f>
• Solá Toni Moragas, Churcher Ian, Lewis William, Stockman Robert A.: Stereoselective aza-Darzens reactions of tert-butanesulfinimines: convenient access to chiral aziridines. Org Biomol Chem 2011, 9, 5034. <http://dx.doi.org/10.1039/c1ob05561e>
• Capriati Vito, Florio Saverio: Anatomy of Long-Lasting Love Affairs with Lithium Carbenoids: Past and Present Status and Future Prospects. Chem Eur J 2010, 16, 4152. <http://dx.doi.org/10.1002/chem.200902870>
• Nagaki Aiichiro, Takizawa Eiji, Yoshida Jun-ichi: Generation and Reactions of Oxiranyllithiums by Use of a Flow Microreactor System. Chem Eur J 2010, 16, 14149. <http://dx.doi.org/10.1002/chem.201000815>
• Robert-Peillard Fabien, Di Chenna Pablo H., Liang Chungen, Lescot Camille, Collet Florence, Dodd Robert H., Dauban Philippe: Catalytic stereoselective alkene aziridination with sulfonimidamides. Tet Asymm 2010, 21, 1447. <http://dx.doi.org/10.1016/j.tetasy.2010.03.032>
• Fantauzzi Simone, Gallo Emma, Caselli Alessandro, Piangiolino Cristiana, Ragaini Fabio, Re Nazzareno, Cenini Sergio: Rearrangement of N-Aryl-2-Vinylaziridines to Benzoazepines and Dihydropyrroles: A Synthetic and Theoretical Study. Chem Eur J 2009, 15, 1241. <http://dx.doi.org/10.1002/chem.200801148>
• Capriati Vito, Florio Saverio, Perna Filippo Maria, Salomone Antonio, Abbotto Alessandro, Amedjkouh Mohamed, Nilsson Lill Sten O.: On the Dichotomic Reactivity of Lithiated Styrene Oxide: A Computational and Multinuclear Magnetic Resonance Investigation. Chem Eur J 2009, 15, 7958. <http://dx.doi.org/10.1002/chem.200900834>
• Concellón José M., Bernad Pablo L., del Solar Virginia, García-Granda Santiago, Díaz M. Rosario: Unusual Totally Selective Cyclodimerization of Epoxides: Synthesis of a Pair of Diastereoisomers of Enantiopure 2,5-Disubstituted-1,4-Dioxanes withC2 Symmetry. Adv Synth Catal 2008, 350, 477. <http://dx.doi.org/10.1002/adsc.200700486>
• Fioravanti Stefania, Marchetti Fabio, Pellacani Lucio, Ranieri Luca, Tardella Paolo A.: Stereoselective aza-MIRC reactions on optically active (E)-nitro alkenes. Tet Asymm 2008, 19, 231. <http://dx.doi.org/10.1016/j.tetasy.2007.12.007>
• Moss Thomas A., Alba Aurelie, Hepworth David, Dixon Darren J.: Efficient base catalyzed alkylation reactions with aziridine electrophiles. Chem Commun 2008, 2474. <http://dx.doi.org/10.1039/b802447b>
• Hodgson David M., Humphreys Philip G., Hughes Steven P.: Widening the Usefulness of Epoxides and Aziridines in Synthesis. ChemInform 2007, 38. <http://dx.doi.org/10.1002/chin.200728270>
• Fantauzzi Simone, Gallo Emma, Caselli Alessandro, Piangiolino Cristiana, Ragaini Fabio, Cenini Sergio: The (Porphyrin)ruthenium-Catalyzed Aziridination of Olefins Using Aryl Azides as Nitrogen Sources. Eur J Org Chem 2007, 2007, 6053. <http://dx.doi.org/10.1002/ejoc.200700678>