Cédric Tresse

2011-2014 Université de Haute Alsace, Mulhouse 
"Cédric Tresse"
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Saint-Auret S, Chany AC, Casarotto V, et al. (2017) Total Syntheses of Mycolactone A/B and its Analogues for the Exploration of the Biology of Buruli Ulcer. Chimia. 71: 836-840
Guissart C, Dolbois A, Tresse C, et al. (2016) A Straightforward Entry to .GAMMA.-Trifluoromethylated Allenamides and Their Synthetic Applications Synlett. 27: 2575-2580
Tresse C, Schweizer S, Bisseret P, et al. (2016) Stereodivergent Hydrosilylation, Hydrostannylation, and Hydrogermylation of α-Trifluoromethylated Alkynes and Their Synthetic Applications Synthesis. 48: 3317-3330
Guenin-Macé L, Baron L, Chany AC, et al. (2015) Shaping mycolactone for therapeutic use against inflammatory disorders. Science Translational Medicine. 7: 289ra85
Schweizer S, Tresse C, Bisseret P, et al. (2015) Stereodivergent hydrogermylations of α-trifluoromethylated alkynes and their applications in cross-coupling reactions. Organic Letters. 17: 1794-7
Blanchard N, Chany AC, Tresse C, et al. (2015) A Walk Across Africa with Captain Grant: Exploring Mycobacterium ulcerans Infection with Mycolactone Analogs Strategies and Tactics in Organic Synthesis. 11: 85-117
Chany AC, Veyron-Churlet R, Tresse C, et al. (2014) Synthetic variants of mycolactone bind and activate Wiskott-Aldrich syndrome proteins. Journal of Medicinal Chemistry. 57: 7382-95
Evano G, Jouvin K, Theunissen C, et al. (2014) Turning unreactive copper acetylides into remarkably powerful and mild alkyne transfer reagents by oxidative umpolung. Chemical Communications (Cambridge, England). 50: 10008-18
Tresse C, Guissart C, Schweizer S, et al. (2014) ChemInform Abstract: Practical Methods for the Synthesis of Trifluoromethylated Alkynes: Oxidative Trifluoromethylation of Copper Acetylides and Alkynes. Cheminform. 45: no-no
Tresse C, Guissart C, Schweizer S, et al. (2014) Practical methods for the synthesis of trifluoromethylated alkynes: Oxidative trifluoromethylation of copper acetylides and alkynes Advanced Synthesis and Catalysis. 356: 2051-2060
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