BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20260216T092104EST-8783vRkSUf@132.216.98.100 DTSTAMP:20260216T142104Z DESCRIPTION:Homogeneous gold catalysis is now recognized as a “convenient t ool for generating molecular complexity” [1] and diversity. [2] The major part of the synthetic chemistry which has been developed so far in this fi eld is intimately linked to the p Lewis acidic property of cationic gold(I ) and gold(III) species.[3] The latter have indeed proven to be particular ly useful catalysts for the functionalization of p systems such as alkynes or allenes by addition of various oxygen\, nitrogen and carbon nucleophil es. In addition to its acidic character\, gold can potentially act as an e lectron donor thus allowing the stabilization of intermediate cationic spe cies and favoring reaction pathways not accessible with other Lewis acids. \n\nDuring the past six years\, we have been actively involved in this dom ain and have developed a series of new methods allowing the formation of v arious hetero- and carbocyclic systems by taking advantage of the singular reactivity of cationic gold species. This lecture will highlight some of our contributions to the field including hydride\, nitrene\, and oxene tra nsfers onto alkynes and allenes.[4]\n\n[1] Fürstner\, A. Chem. Soc. Rev. 2 009\, 38\, 3208.\n\n \n\n[2] Jimenez-Nunez\, E.\; Echavarren\, A. M. Chem. Commun. 2007\, 333.\n\n[3] Selected reviews: (a) Gorin\, D. J.\; Toste\, F. D. Chem. Rev. 2008\, 108\, 3351\; (b) Hashmi\, A. S. K. Chem. Rev. 2007 \, 107\, 3180\; (c) Fürstner\, A.\; Davies\, P. W. Angew. Chem. Int. Ed. 2 007\, 46\, 3410.\n\n[4] For recent contributions from our group\, see: a) Prechter\, A.\; Henrion\, G.\; Faudot dit Bel\, P.\; Gagosz\, F. Angew. Ch em. Int. Ed. 2014\, 53\, 4959\; b) Gronnier\, C. \; Boissonnat\, G. Gagosz \, F. Org. Lett. 2013\, 15\, 4234 \; c) Ziping\, C.\; Gagosz\, F. Angew. C hem. Int. Ed. 2013\, 52\, 9014\; d) Henrion\, G.\; Chavas\, T. E. J.\; Le Goff\, X.\; Gagosz\, F. Angew. Chem. Int. Ed. 2013\, 52\, 6277\; e) Gronni er\, C.\; Kramer\, S.\; Odabachian\, Y.\; Gagosz F. J. Am. Chem. Soc. 2012 \, 134\, 828.\n DTSTART:20151026T180000Z DTEND:20151026T193000Z LOCATION:Ruttan Room\, Maass Chemistry Building\, CA\, QC\, Montreal\, H3A 0B8\, 801 rue Sherbrooke Ouest SUMMARY:CCVC Seminar: Fabien Gagosz – Gold catalyzed reactions for organic synthesis URL:/chemistry/channels/event/ccvc-seminar-fabien-gago sz-gold-catalyzed-reactions-organic-synthesis-256273 END:VEVENT END:VCALENDAR