Publications 2013 «Bottleable (Amino)(Carboxy) Radicals Derived from Cyclic (Alkyl)(Amino) Carbenes» J. K. Mahoney, D. Martin, C. E. Moore, A. L. Rheingold, G. Bertrand, J. Am. Chem. Soc. 2013, 135, 18766-18769. DOI: 10.1021/ja4104765  «β- and α-Hydride Abstraction in Gold(I) Alkyl Complexes» Ung, G Bertrand, Angew. Chem. Int. Ed. 2013, 52, 11388-11391. DOI: 10.1002/anie.201306550  «Crystalline, Lewis Base-Free, Cationic Phosphoranimines (Iminophosphonium Salts)» Dielmann, C. E. Moore, A. L. Rheingold, G. Bertrand, J. Am. Chem. Soc. 2013, 14071–14073. DOI: 10.1021/ja4080979  « Experimental and Computational Studies of Anti-Bredt Amidinium Salts » Martin, N. Lassauque, F. Steinmann, G. Manuel, G. Bertrand, Chem. Eur. J. 2013, 19, 14895-14901. DOI: 10.1002/chem.201302474  « Carbodicarbenes, Carbon(0) Derivatives, Can Dimerize » A. Ruiz, M. Melaimi, G. Bertrand, Chem. Asian J. 2013, 8, 2940-2942 DOI: 10.1002/asia.201300887  «Isolation of Neutral Mono- and Dinuclear Gold Complexes of Cyclic (Alkyl)(amino)carbenes» D. S. Weinberger, M. Melaimi, C. E. Moore, A. L. Rheingold, G. Frenking, P. Jerabek, G. Bertrand, Angew. Chem. Int. Ed. 2013, 52, 8964-8967. DOI: 10.1002/anie.201304820  «Deprotonation of a Borohydride: Synthesis of a Carbene-Stabilized Boryl Anion» D. A. Ruiz, G. Ung, M. Melaimi, G. Bertrand, Angew. Chem. Int. Ed. 2013, 52, 7590-7592. DOI: 10.1002/anie.201303457  « An Air-Stable Oxyallyl Radical Cation » Martin, C. E. Moore, A. L. Rheingold, G. Bertrand, Angew. Chem. Int. Ed. 2013, 52, 7014-7017. DOI: 10.1002/anie.201302841  « Carbene-Stabilized Main Group Radicals and Radical Ions » C. D. Martin, M. Soleilhavoup, G. Bertrand, Chem. Sci., 2013, 4, 3020-3030. DOI:10.1039/C3SC51174J  « Exploring the reactivity of white phosphorus with electrophilic carbenes: synthesis of a P4 cage and P8 clusters» C. D. Martin, C. M. Weinstein, C. E. Moore, A. L. Rheingold, G. Bertrand, Chem. Commun. 2013, 4486-4488. DOI: 10.1039/C3CC42041H  « Anti-Bredt N-Heterocyclic Carbene: an Efficient Ligand for the Gold(I)-Catalyzed Hydroamination of Terminal Alkynes with Parent Hydrazine » M. J. Lopez-Gomez, D. Martin, G. Bertrand Chem. Commun. 2013, 4483-4485. DOI: 10.1039/C3CC41279B   graphical design: Maria Lopez-Gomez and Sara Leal Regueiro « 31P NMR Chemical Shifts of Carbene–Phosphinidene Adducts as an Indicator of the π-Accepting Properties of Carbenes » O. Back, M. Henry-Ellinger, C. D. Martin, D. Martin, G. Bertrand, Angew. Chem. Int. Ed. 2013, 52, 2939-2943. DOI: 10.1002/anie.201209109  « Gold(III)- versus Gold(I)-induced cyclization: synthesis of six-membered mesoionic carbene and acyclic (aryl)(heteroaryl) carbene complexes» G. Ung, M. Soleilhavoup, G. Bertrand, Angew. Chem. Int. Ed. 2013, 52, 758-761, DOI: 10.1002/anie.201207961  « Synthesis and characterization of a pyrazolium bearing N-heterocyclic carbene–palladium(II) complex » E. Giziroglu, B. Donnadieu, G. Bertrand, J. Organomet. Chem. 2013, 724, 251-254. DOI: 10.1016/j.jorganchem.2012.11.021  « Les carbènes stables: Des curiosités de laboratoire devenus des outils puissants. » Soleilhavoup, M. Melaimi, D. Martin, G. Bertrand, Actualité Chimique 2013, 370, 20-27. link  http://pubs.acs.org/doi/abs/10.1021/ja4104765http://dx.doi.org/10.1002/anie.201306550http://dx.doi.org/10.1021/ja4080979http://dx.doi.org/10.1002/chem.201302474http://onlinelibrary.wiley.com/doi/10.1002/asia.201300887/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/anie.201304820/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/anie.201303457/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/anie.201302841/abstracthttp://pubs.rsc.org/en/content/articlelanding/2013/sc/c3sc51174jhttp://pubs.rsc.org/en/content/articlelanding/2013/cc/c3cc42041hhttp://dx.doi.org/10.1039/C3CC41279Bhttp://onlinelibrary.wiley.com/doi/10.1002/anie.201209109/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/anie.201207961/abstracthttp://dx.doi.org/10.1016/j.jorganchem.2012.11.021http://www.lactualitechimique.org/larevue_article.php?cle=3157shapeimage_1_link_0shapeimage_1_link_1shapeimage_1_link_2shapeimage_1_link_3shapeimage_1_link_4shapeimage_1_link_5shapeimage_1_link_6shapeimage_1_link_7shapeimage_1_link_8shapeimage_1_link_9shapeimage_1_link_10shapeimage_1_link_11shapeimage_1_link_12shapeimage_1_link_13shapeimage_1_link_14

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