Jean-Marc Campagne

ICSN CNRS, Paris, Île-de-France, France 
"Jean-Marc Campagne"
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Mudráková B, Marcia de Figueiredo R, Campagne JM, et al. (2023) Asymmetric tandem conjugate addition and reaction with carbocations on acylimidazole Michael acceptors. Beilstein Journal of Organic Chemistry. 19: 881-888
Sahtel S, Maamer CB, Besbes R, et al. (2022) Straightforward synthesis of various chiral pyrimidines bearing a stereogenic center adjacent to the C-2 position, including C-terminal peptide isosteres. Amino Acids
Tosi E, Campagne JM, de Figueiredo RM. (2022) Amine Activation: "Inverse" Dipeptide Synthesis and Amide Function Formation through Activated Amino Compounds. The Journal of Organic Chemistry. 87: 12148-12163
Hubert P, Seibel E, Beemelmanns C, et al. (2020) Stereoselective Construction of (E,Z)‐1,3‐Dienes and Its Application in Natural Product Synthesis Advanced Synthesis & Catalysis
Lauberteaux J, Lebrun A, van der Lee A, et al. (2019) Iron-Catalyzed Enantioselective Intramolecular Inverse Electron-Demand Hetero Diels-Alder Reactions: An Access to Bicyclic Dihydropyran Derivatives. Organic Letters
Pichon D, Soleilhavoup M, Morvan J, et al. (2019) The debut of chiral cyclic (alkyl)(amino)carbenes (CAACs) in enantioselective catalysis. Chemical Science. 10: 7807-7811
Pereira de Sant'Ana D, de Oliveira Rezende Júnior C, Campagne JM, et al. (2019) Synthetic Studies toward the Total Synthesis of Tautomycetin. The Journal of Organic Chemistry. 84: 12344-12357
Aguesseau-Kondrotas J, Simon M, Legrand B, et al. (2019) Prospect of thiazole-based γ-peptide foldamers in enamine catalysis - exploration of the Nitro-Michael addition. Chemistry (Weinheim An Der Bergstrasse, Germany)
Lauberteaux J, Crévisy C, Baslé O, et al. (2019) Copper-Catalyzed Asymmetric Conjugate Additions of Bis(pinacolato)diboron and Dimethylzinc to Acyl- N-methylimidazole Michael Acceptors: A Highly Stereoselective Unified Strategy for 1,3,5,... n (OH, Me) Motif Synthesis. Organic Letters. 21: 1872-1876
Lauberteaux J, Pichon D, Baslé O, et al. (2019) Acyl-Imidazoles A Privileged Ester Surrogate for Enantioselective Synthesis Chemcatchem. 11: 5705-5722
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