Publications 2016 «The Transition Metal-like Behavior of Main Group Elements: Ligand Exchange at a Phosphinidene» Max M. Hansmann and Guy Bertrand, J. Am. Chem. Soc. 2016, 138, 15885-15888. DOI: 10.1021/jacs.6b11496 «Nucleophilic T-shaped (LXL)Au(I)-Pincer Complexes: Protonation and Alkylation» George Kleinhans, Max M. Hansmann,  Gregorio Guisado-Barrios, David C. Liles, Guy Bertrand, Daniela I. Bezuidenhout, J. Am. Chem. Soc. 2016, 138, 15873-15876. DOI: 10.1021/jacs.6b11359 «NHC-CAAC Heterodimers with Three Stable Oxidation States» Dominik Munz, Jiaxiang Chu, Mohand Melaimi, Guy Bertrand, Angew. Chem. Int. Ed., 2016, 55, 12886-12890. DOI: 10.1002/anie.201607537 «Catalyst-Free Dehydrocoupling of Amines, Alcohols, and Thiols with Pinacol Borane and 9-Borabicyclononane (9-BBN)» Erik A. Romero, Jesse L. Peltier, Rodolphe Jazzar, Guy Bertrand, Chem. Commun., 2016, 52, 10563-10565. DOI: 10.1039/C6CC06096J «Singlet (Phosphino)phosphinidenes are Electrophilic» Max M. Hansmann, Rodolphe Jazzar, Guy Bertrand, J. Am. Chem. Soc., 2016, 138, 8356-8359. DOI: 10.1021/jacs.6b04232 «Synthesis of Hemilabile Cyclic (Alkyl)(amino)carbenes (CAACs) and Applications in Organometallic Chemistry» Jiaxiang Chu, Dominik Munz, Rodolphe Jazzar, Mohand Melaimi, Guy Bertrand, J. Am. Chem. Soc., 2016, 138, 7884-7887. DOI: 10.1021/jacs.6b05221 «A Singlet Phosphinidene Stable at Room Temperature» Liu Liu, David A. Ruiz, Dominik Munz, Guy Bertrand, Chem, 2016, 1, 147-153. DOI: 10.1016/j.chempr.2016.04.001 «Generalization of the Copper to Late-Transition-Metal Transmetallation to Carbenes beyond N-Heterocyclic Carbenes» Dr. Yannick D. Bidal, Orlando Santoro, Dr. Mohand Melaimi, Dr. David B. Cordes, Prof. Alexandra M. Z. Slawin, Prof. Guy Bertrand, Dr. Catherine S. J. Cazin, Chem. Eur. J., 2016, 22, 9404-9409. DOI: 10.1002/chem.201601254 «Room temperature hydroamination of alkynes with anilines catalyzed by anti-Bredt di(amino)carbene gold(I) complexes» Xingbang Hu, David Martin, and Guy Bertrand, New J. Chem., 2016, 40, 5993-5996. DOI: 10.1039/C6NJ00980H «N-Heterocyclic Carbenes as Promotors for the Rearrangement of Phosphaketenes to Phosphaheteroallenes: A Case Study for OCP to OPC Constitutional Isomerism» Dr. Zhongshu Li, Dr. Xiaodan Chen, Dr. Zoltán Benkő, Liu Liu, Dr. David A. Ruiz, Jesse L. Peltier, Prof. Dr. Guy Bertrand, Prof. Dr. Chen-Yong Su, Prof. Dr. Hansjörg Grützmacher, Angew. Chem. Int. Ed., 2016, 55, 6018-6022. DOI: 10.1002/anie.201600903 «A Ruthenium Catalyst for Olefin Metathesis Featuring an Anti-Bredt N-Heterocyclic Carbene Ligand» David Martin, Vanessa M. Marx, Robert H. Grubbs, and Guy Bertrand, Adv. Synth. Catal., 2016, 358, 965–969. DOI: 10.1002/adsc.201501140 «Synthesis of a Carbodicyclopropenylidene: A Carbodicarbene based Solely on Carbon» Conor Pranckevicius, Liu Liu, Prof. Dr. Guy Bertrand, Prof. Dr. Douglas W. Stephan, Angew. Chem. Int. Ed. 2016, 55, 5536-5540. DOI: 10.1002/anie.201600765 «Isolation of Au-, Co-η1PCO and Cu-η2PCO complexes, conversion of an Ir–η1PCO complex into a dimetalladiphosphene, and an interaction-free PCO anion» Liu Liu, David A. Ruiz, Fatme Dahcheh, Guy Bertrand, Riccardo Suter, Aaron M. Tondreau and Hansjörg Grützmacher, Chem. Sci. 2016, 7, 2335-2341. DOI: 10.1039/C5SC04504E  «A rhodium(I)–oxygen adduct as a selective catalyst for one-pot sequential alkyne dimerization-hydrothiolation tandem reactions» George Kleinhans, Gregorio Guisado-Barrios, David C. Liles, Guy Bertrand, Daniela I. Bezuidenhout, Chem. Comm., 2016, 52, 3504-3507. DOI: 10.1039/C6CC00029K «Ancillary Ligand-Free Copper Catalysed Hydrohydrazination of Terminal Alkynes with NH2NH2» Jesse L Peltier, Rodolphe Jazzar, Melaimi Mohand and Guy Bertrand, Chem. Comm. 2016, 52, 2733-2735. DOI: 10.1039/C5CC10427K  «Isolation of cationic and neutral (allenylidene)(carbene) and bis(allenylidene)gold Complexes» L. Jin, M. Melaimi, A. Kostenko, M. Karni, Y. Apeloig, C. E. Moore, A. L. Rheingold and G. Bertrand, Chem. Sci. 2016, 7, 150-154. DOI: 10.1039/C5SC03654B  http://pubs.acs.org/doi/abs/10.1021/jacs.6b11496http://pubs.acs.org/doi/abs/10.1021/jacs.6b11359http://onlinelibrary.wiley.com/doi/10.1002/anie.201607537/fullhttp://pubs.rsc.org/en/content/articlelanding/2016/cc/c6cc06096j#!divAbstracthttp://pubs.acs.org/doi/abs/10.1021/jacs.6b04232http://pubs.acs.org/doi/abs/10.1021/jacs.6b05221http://pubs.acs.org/doi/abs/10.1021/jacs.6b05221http://dx.doi.org/10.1016/j.chempr.2016.04.001http://dx.doi.org/10.1016/j.chempr.2016.04.001http://onlinelibrary.wiley.com/doi/10.1002/chem.201601254/fullhttp://pubs.rsc.org/en/Content/ArticleLanding/2016/NJ/C6NJ00980H#!divAbstracthttp://onlinelibrary.wiley.com/doi/10.1002/anie.201600903/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/adsc.201501140/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/anie.201600765/fullhttp://pubs.rsc.org/en/content/articlelanding/2016/sc/c5sc04504e#!divAbstracthttp://pubs.rsc.org/en/Content/ArticleLanding/2016/CC/C6CC00029K#!divAbstracthttp://pubs.rsc.org/en/content/articlelanding/2016/cc/c5cc10427k#!divAbstracthttp://pubs.rsc.org/en/content/articlelanding/2015/sc/c5sc03654b#!divAbstractshapeimage_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_14shapeimage_1_link_15shapeimage_1_link_16shapeimage_1_link_17

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