Wilfried Raimondi
Affiliations: | Aix Marseille University |
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Bonne D, Rodriguez J, Becerra D, et al. (2016) Enantioselective Organocatalyzed Consecutive Synthesis of Alkyl 4,5-Dihydrofuran-2-carboxylates from α-Keto Esters and (Z)-β-Chloro-β-nitrostyrenes Synthesis. 49: 195-201 |
Xu K, Raimondi W, Bury T, et al. (2015) Enantioselective formation of tertiary and quaternary allylic C-N bonds via allylation of tetrazoles. Chemical Communications (Cambridge, England). 51: 10861-3 |
Bugaut X, Bonne D, Raimondi W, et al. (2013) Activation of 1,2- and 1,3-Ketoamides with Thiourea Organocatalyst for the Enantioselective Domino Synthesis of Functionalized Cyclohexanes Synthesis. 45: 1659-1666 |
Bonne D, Rodriguez J, Goudedranche S, et al. (2013) Enantioselective Organocatalyzed Domino Synthesis of Six-Membered Carbocycles Synthesis. 45: 1909-1930 |
Raimondi W, Sanchez Duque MdM, Goudedranche S, et al. (2013) ChemInform Abstract: Activation of 1,2- and 1,3-Ketoamides with Thiourea Organocatalyst for the Enantioselective Domino Synthesis of Functionalized Cyclohexanes. Cheminform. 44: no-no |
Goudedranche S, Raimondi W, Bugaut X, et al. (2013) ChemInform Abstract: Enantioselective Organocatalyzed Domino Synthesis of Six-Membered Carbocycles Cheminform. 44: no-no |
Mailhol D, del Mar Sanchez Duque M, Raimondi W, et al. (2013) ChemInform Abstract: Enantioselective Organocatalytic Michael Addition of Cyclobutanones to Nitroalkenes. Cheminform. 44: no-no |
Raimondi W, Dauzonne D, Constantieux T, et al. (2013) ChemInform Abstract: Expeditious, Metal-Free, Domino, Regioselective Synthesis of Highly Substituted 2-Carbonyl- and 2-Phosphorylfurans by Formal [3 + 2] Cycloaddition. Cheminform. 44: no-no |
Raimondi W, Bonne D, Rodriguez J. (2012) Asymmetric transformations involving 1,2-dicarbonyl compounds as pronucleophiles. Chemical Communications (Cambridge, England). 48: 6763-75 |
Raimondi W, Bonne D, Rodriguez J. (2012) 1,2-Dicarbonyl compounds as pronucleophiles in organocatalytic asymmetric transformations. Angewandte Chemie (International Ed. in English). 51: 40-2 |