Sami Lakhdar
Affiliations: | 2013- | CNRS, Paris, Île-de-France, France |
Area:
Organic chemistryGoogle:
"Sami Lakhdar"Mean distance: 8.62 | S | N | B | C | P |
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Publications
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Inial A, Morlet-Savary F, Lalevée J, et al. (2020) Visible-Light-Mediated Access to Phosphate Esters. Organic Letters. 22: 4404-4407 |
Gasnot J, Botella C, Comesse S, et al. (2020) Taming the reactivity of Phosphiranium salts: Site-selective C-centered-Ring Opening for Direct Synthesis of Phosphinoethylamines. Angewandte Chemie (International Ed. in English) |
Dalla V, Taillier C, Gasnot J, et al. (2020) Access to Stable Quaternary Phosphiranium Salts by P-Alkylation and P-Arylation of Phosphiranes Synlett. 31: 883-888 |
Kirschner J, Paillard J, Bouzrati-Zerelli M, et al. (2019) Aryliodonium Ylides as Novel and Efficient Additives for Radical Chemistry: Example in Camphorquinone (CQ)/Amine Based Photoinitiating Systems. Molecules (Basel, Switzerland). 24 |
Pal S, Gaumont AC, Lakhdar S, et al. (2019) Diphenyliodonium Ion/EtN Promoted Csp2-H Radical Phosphorylation of Enamides. Organic Letters |
Pasturaud K, Rkein B, Sanselme M, et al. (2019) The facile dearomatization of nitroaromatic compounds using lithium enolates of unsaturated ketones in conjugate additions and (4+2) formal cycloadditions. Chemical Communications (Cambridge, England) |
Quint V, Chouchène N, Askri M, et al. (2019) Visible-light-mediated α-phosphorylation of N-aryl tertiary amines through the formation of electron-donor–acceptor complexes: synthetic and mechanistic studies Organic Chemistry Frontiers. 6: 41-44 |
Lecroq W, Bazille P, Morlet-Savary F, et al. (2018) Visible-Light-Mediated Metal-Free Synthesis of Aryl Phosphonates: Synthetic and Mechanistic Investigations. Organic Letters |
Harrison-Marchand A, Guang J, Duwald R, et al. (2018) Synthesis and Identification of Aryl and Alkyl Gem-Dilithium Phosphido-Boranes: A Boost to the Chemistry of Phosphandiides. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Rousée K, Pannecoucke X, Gaumont AC, et al. (2017) Transition metal-free stereospecific access to (E)-(1-fluoro-2-arylvinyl)phosphine borane complexes. Chemical Communications (Cambridge, England) |