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Gwilherm Evano

Professor Gwilherm Evano

Research in the Evano group focuses on three areas: natural product synthesis, copper catalysis, and the chemistry of hetero-substituted alkynes. In particular, they developed a set of efficient and robust procedures, mostly based on copper catalysis, for the synthesis of ynamides starting from readily available starting materials. They have also explored the synthetic potential of these bench-stable reagents which were shown to be remarkable substrates and building blocks, notably in anionic and cationic chemistry. By exploiting and rationalizing the singular and remarkable reactivity of ynamides, reaction pathways that could not be accessed with regular alkynes could be exploited to access various nitrogen-containing molecules, including complex and otherwise hardly accessible nitrogen heterocycles, with high levels of efficiency. The Evano group is currently continuing its work on the chemistry of ynamides, with an emphasis in asymmetric synthesis, and its extension to other classes of hetero-substituted acetylenes.

Evano Group Website

Recent papers from the Evano Group

Evano G, Coste A, Jouvin K. 2010. Ynamides: Versatile Tools in Organic Synthesis. Angewandte Chemie International Edition. 49(16):2840-2859.
Gati W, Rammah MM, Rammah MB, Couty F, Evano G. 2012. De Novo Synthesis of 1,4-Dihydropyridines and Pyridines. J. Am. Chem. Soc.. 134(22):9078-9081.
Theunissen C, Métayer B, Henry N, Compain G, Marrot J, Martin-Mingot A, Thibaudeau S, Evano G. 2014. Keteniminium Ion-Initiated Cascade Cationic Polycyclization. J. Am. Chem. Soc.. 136(36):12528-12531.
Products available from the Evano Group


  • Organic Synthetic Chemistry
  • Catalysis

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