Thierry Jousseaume - Publications

Affiliations: 
2006-2009 Université Paris-Saclay, Gif-sur-Yvette, Essonne, France 

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 Suri M, Jousseaume T, Neumann JJ, Glorius F. An efficient copper-catalyzed formation of highly substituted pyrazoles using molecular oxygen as the oxidant Green Chemistry. 14: 2193-2196. DOI: 10.1039/C2Gc35476D  0.464
2012 Jousseaume T, Retailleau P, Chabaud L, Guillou C. Studies on the asymmetric Birch reductive alkylation to access spiroimines Tetrahedron Letters. 53: 1370-1372. DOI: 10.1016/J.Tetlet.2012.01.008  0.664
2011 Duroure L, Jousseaume T, Aráoz R, Barré E, Retailleau P, Chabaud L, Molgó J, Guillou C. 6,6-Spiroimine analogs of (-)-gymnodimine A: synthesis and biological evaluation on nicotinic acetylcholine receptors. Organic & Biomolecular Chemistry. 9: 8112-8. PMID 22024965 DOI: 10.1039/C1Ob06257C  0.642
2011 Jousseaume T, Wurz NE, Glorius F. Highly enantioselective synthesis of α-amino acid derivatives by an NHC-catalyzed intermolecular Stetter reaction. Angewandte Chemie (International Ed. in English). 50: 1410-4. PMID 21290524 DOI: 10.1002/Anie.201006548  0.643
2011 Chabaud L, Jousseaume T, Retailleau P, Guillou C. ChemInform Abstract: Vinylogous Mukaiyama-Michael Reactions Between 2-Silyloxyfurans and Cyclic Enones or Unsaturated Oxo Esters. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201107134  0.652
2011 Jousseaume T, Wurz NE, Glorius F. Hoch enantioselektive Synthese von α-Aminosäurederivaten durch NHC-katalysierte intermolekulare Stetter-Reaktion Angewandte Chemie. 123: 1446-1450. DOI: 10.1002/Ange.201006548  0.513
2010 Chabaud L, Jousseaume T, Retailleau P, Guillou C. Vinylogous Mukaiyama-Michael Reactions between 2-Silyloxyfurans and Cyclic Enones or Unsaturated Oxo Esters European Journal of Organic Chemistry. 2010: 5471-5481. DOI: 10.1002/Ejoc.201000504  0.667
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