Sophie Rousseaux, PhD

Affiliations: 
2015 University of Oxford, Oxford, United Kingdom 
 2015- University of Toronto, Toronto, ON, Canada 
Area:
Catalysis, reaction mechanisms, organmetallic chemistry
Website:
http://www.chem.utoronto.ca/wp/rousseaux/
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"Sophie Rousseaux"
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Publications

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McDonald TR, Turner JA, Gabbey AL, et al. (2024) Synthesis of Borylated (Aminomethyl)cyclopropanes Using C-Bisnucleophiles. Organic Letters
Michel NWM, Gabbey AL, Edjoc RK, et al. (2024) Nickel-Catalyzed Reductive Arylation of Redox Active Esters for the Synthesis of α-Aryl Nitriles: Investigation of a Chlorosilane Additive. The Journal of Organic Chemistry
Gabbey AL, Michel NWM, Hughes JME, et al. (2022) Synthesis of α-Aryl Secondary Amides via Nickel-Catalyzed Reductive Coupling of Redox-Active Esters. Organic Letters
Mills LR, Graham J, Patel P, et al. (2019) Ni-Catalyzed Reductive Cyanation of Aryl Halides and Phenol Derivatives via Transnitrilation. Journal of the American Chemical Society
Michel NWM, Jeanneret ADM, Kim H, et al. (2018) Nickel-Catalyzed Cyanation of Benzylic and Allylic Pivalate Esters. The Journal of Organic Chemistry
Liu S, Kondratuk DV, Rousseaux SA, et al. (2015) Caterpillar Track Complexes in Template-Directed Synthesis and Correlated Molecular Motion. Angewandte Chemie (Weinheim An Der Bergstrasse, Germany). 127: 5445-5449
Rousseaux SA, Gong JQ, Haver R, et al. (2015) Self-Assembly of Russian Doll Concentric Porphyrin Nanorings. Journal of the American Chemical Society
Liu S, Kondratuk DV, Rousseaux SA, et al. (2015) Caterpillar track complexes in template-directed synthesis and correlated molecular motion. Angewandte Chemie (International Ed. in English). 54: 5355-9
Rousseaux S, Vrancken E, Campagne JM. (2012) Chiral aryl-copper(III) electrophiles: new opportunities in catalytic enantioselective arylations and domino processes. Angewandte Chemie (International Ed. in English). 51: 10934-5
Rousseaux S, Liégault B, Fagnou K. (2012) Palladium(0)-catalyzed cyclopropane C-H bond functionalization: Synthesis of quinoline and tetrahydroquinoline derivatives Chemical Science. 3: 244-248
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