Catherine Guillou

Affiliations: 
Institut de Chimie des Substances Naturelles 
Area:
Medicinal Chemistry
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"Catherine Guillou"
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Publications

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Bayles T, Guillou C. (2022) Trifluoroethanol Promoted Castagnoli-Cushman Cycloadditions of Imines with Homophthalic Anhydride. Molecules (Basel, Switzerland). 27
Peneau A, Tricart Q, Guillou C, et al. (2018) Mild rhodium(iii)-catalyzed intramolecular annulation of benzamides with allylic alcohols to access azepinone derivatives. Chemical Communications (Cambridge, England)
Peneau A, Retailleau P, Guillou C, et al. (2018) Rhodium(III)-Catalyzed Synthesis of Spiropiperidine Derivatives via C-H Activation. The Journal of Organic Chemistry. 83: 2324-2340
Peneau A, Guillou C, Chabaud L. (2018) Recent Advances in [Cp*MIII ] (M = Co, Rh, Ir)-Catalyzed Intramolecular Annulation Through C-H Activation European Journal of Organic Chemistry. 2018: 5777-5794
Chabaud L, Raynal Q, Barre E, et al. (2016) ChemInform Abstract: Rhodium(III)-Catalyzed Synthesis of Aryl Spirocycles by Aromatic C-H Activation/Intramolecular Heck-Type Reaction. Cheminform. 47
Hromjakova T, Retailleau P, Grimaud L, et al. (2016) ChemInform Abstract: Hypervalent-Iodine-Mediated Synthesis of 1,2-Dispirodienones: Experimental and Theoretical Investigations. Cheminform. 47
Hromjakova T, Retailleau P, Grimaud L, et al. (2015) Hypervalent-Iodine-Mediated Synthesis of 1,2-Dispirodienones: Experimental and Theoretical Investigations European Journal of Organic Chemistry. 2015: 7494-7503
Rambla M, Duroure L, Chabaud L, et al. (2015) ChemInform Abstract: Enantioselective Synthesis of Spiroimines by Asymmetric Decarboxylative Alkylation/Isomerization/[3 + 2]-Cycloaddition Reaction of Azidoalkenes. Cheminform. 46: no-no
Chabaud L, Raynal Q, Barre E, et al. (2015) Rhodium(III)-Catalyzed Synthesis of Aryl Spirocycles by Aromatic CH Activation/Intramolecular Heck-Type Reaction Advanced Synthesis & Catalysis. 357: 3880-3884
Jusseau X, Chabaud L, Guillou C. (2014) Synthesis of γ-butenolides and α,β-unsaturated γ-butyrolactams by addition of vinylogous nucleophiles to Michael acceptors Tetrahedron. 70: 2595-2615
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