Jean-Luc Parrain

Chimie Aix Marseille Université 
"Jean-Luc Parrain"
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Saidah M, Mardjan MID, Masson G, et al. (2022) Enantioselective Construction of Tetrasubstituted Carbon Stereocenters via Chiral Phosphoric Acid-Catalyzed Friedel-Craft Alkylation of Indoles with 5-Substituted Hydroxybutyrolactams. Organic Letters. 24: 5298-5303
Manick AD, Salgues B, Parrain JL, et al. (2020) Access to Fluorenones Using Benzocyclopentynone Surrogate as Partner for the [2 + 2 + 2] Cycloaddition Reaction. Organic Letters. 22: 1894-1898
Mardjan MID, Mayooufi A, Parrain J, et al. (2020) Straightforward Access to a Great Diversity of Complex Biorelevant γ-Lactams Thanks to a Tunable Cascade Multicomponent Process Organic Process Research & Development. 24: 606-614
Vivien A, Bartoli A, Parrain J, et al. (2020) Regioselective 1,6-conjugate addition of organocuprate reagents to γ-alkylidenebutenolides Tetrahedron Letters. 61: 151472
Nava P, Toure M, Abdou Mohamed A, et al. (2019) Investigation of the rhodium-catalyzed hydroboration of NHC-boranes: the role of alkene coordination and the origin of enantioselectivity. Dalton Transactions (Cambridge, England : 2003)
Delorme M, Punter A, Oliveira R, et al. (2019) When cobalt-mediated [2 + 2 + 2] cycloaddition reaction dares go astray: synthesis of unprecedented cobalt(iii)-complexes. Dalton Transactions (Cambridge, England : 2003)
Aupic C, Abdou Mohamed A, Figliola C, et al. (2019) Highly diastereoselective preparation of chiral NHC-boranes stereogenic at the boron atom. Chemical Science. 10: 6524-6530
Commeiras L, Mardjan MID, Parrain J. (2018) Strategies To Access γ-Hydroxy-γ-butyrolactams Synthesis. 50: 1175-1198
Bressy C, Merad J, Borkar P, et al. (2017) Double Catalytic Kinetic Resolution (DoCKR) of Acyclic anti-1,3-Diols using Additive Horeau Amplification. Angewandte Chemie (International Ed. in English)
Dousset M, Parrain J, Chouraqui G. (2017) Intriguing Electrophilic Reactivity of Donor-Acceptor Cyclopropanes: Experimental and Theoretical Studies European Journal of Organic Chemistry. 2017: 5238-5245
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