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Rachid Baati

Observed names: Baati, R., Baati, Rachid, R Baati, R. BAATI, R. Baati
Observed institutions: Scripps Research Institute, Centre National de la Recherche Scientifique, Stockholm University, Southern Methodist University, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, University of California San Diego, University of Oxford, Laboratoire des Matériaux Surfaces et Procédés pour la Catalyse, Laboratoire de Chémo-biologie synthétique et thérapeutique, CEA Paris-Saclay, Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé, Pierre Fabre (France), Paris Biotech Santé, Université de Rouen Normandie, Université de Strasbourg, The University of Texas Southwestern Medical Center
ORCID: 0000-0002-5820-5274
Observed ORCID: 0000-0002-5820-5274
OpenAlex ID: A5038896040
Reactivators of Acetylcholinesterase Inhibited by Organophosphorus Nerve Agents
2012 · Guillaume Mercey, Tristan Verdelet, et al. · Accounts of Chemical Research · 420
Stereocontrolled Total Synthesis of Apicularen A and Its Δ17,18 Z Isomer
2002 · K. C. Nicolaou, David W. Kim, et al. · Angewandte Chemie International Edition · 123
First efficient uncharged reactivators for the dephosphylation of poisoned human acetylcholinesterase
2011 · Guillaume Mercey, Tristan Verdelet, et al. · Chemical Communications · 112
Selective Irreversible Chemical Tagging of Cysteine with 3-Arylpropiolonitriles
2014 · Oleksandr Koniev, Geoffray Leriche, et al. · Bioconjugate Chemistry · 98
Design, synthesis and biological evaluation of novel tetrahydroacridine pyridine- aldoxime and -amidoxime hybrids as efficient uncharged reactivators of nerve agent-inhibited human acetylcholinesterase
2014 · Maria Kliachyna, Gianluca Santoni, et al. · European Journal of Medicinal Chemistry · 84
Design, synthesis and evaluation of new α-nucleophiles for the hydrolysis of organophosphorus nerve agents: application to the reactivation of phosphorylated acetylcholinesterase
2011 · Géraldine Saint-André, Maria Kliachyna, et al. · Tetrahedron · 78
Potent 3‐Hydroxy‐2‐Pyridine Aldoxime Reactivators of Organophosphate‐Inhibited Cholinesterases with Predicted Blood–Brain Barrier Penetration
2018 · Tamara Zorbaz, Anissa Braïki, et al. · Chemistry - A European Journal · 76
TBD‐Catalyzed Direct 5‐ and 6‐enolexo Aldolization of Ketoaldehydes
2008 · Cynthia Ghobril, Cyrille Sabot, et al. · European Journal of Organic Chemistry · 68
Structure-Based Optimization of Nonquaternary Reactivators of Acetylcholinesterase Inhibited by Organophosphorus Nerve Agents
2018 · Gianluca Santoni, Julien de Sousa, et al. · Journal of Medicinal Chemistry · 64
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Total Synthesis and Biological Evaluation of (−)Apicularen A and Analogues Thereof
2003 · K. C. Nicolaou, David W. Kim, et al. · Chemistry - A European Journal · 63
Total Synthesis of (±)-Halomon by a Johnson-Claisen Rearrangement
1998 · Thierry Schlama, Rachid Baati, et al. · Angewandte Chemie International Edition · 62
A HTS Assay for the Detection of Organophosphorus Nerve Agent Scavengers
2010 · Ludivine Louise‐Leriche, Emilia Pǎunescu, et al. · Chemistry - A European Journal · 61
Phenyltetrahydroisoquinoline–Pyridinaldoxime Conjugates as Efficient Uncharged Reactivators for the Dephosphylation of Inhibited Human Acetylcholinesterase
2012 · Guillaume Mercey, Julien Renou, et al. · Journal of Medicinal Chemistry · 59
Syntheses and in vitro evaluations of uncharged reactivators for human acetylcholinesterase inhibited by organophosphorus nerve agents
2012 · Julien Renou, Guillaume Mercey, et al. · Chemico-Biological Interactions · 59
Model Studies Towards Azadirachtin: Part 2. Construction of the Crowded C8bC14 Bond by Transition Metal Chemistry We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), the Skaggs Institute for Chemical Biology, a predoctoral fellowship from the Division of Organic Chemistry of the American Chemical Society sponsored by Novartis (to A.J.R.), postdoctoral fellowships from Bayer AG (to M.F.), and Association pour la Recherche sur le Cancer (to R.B.), and grants from Abbott Laboratories, ArrayBiopharma, Bayer, Boehringer Ingelheim, DuPont, Glaxo, Hoffmann-LaRoche, Merck, Novartis, Pfizer, and Schering Plough.
2002 · K. C. Nicolaou, A. J. Roecker, et al. · Angewandte Chemie International Edition · 53
A Convenient Synthesis of 2-Tetrahydrofuranyl Ethers
2000 · Rachid Baati, Alain Valleix, et al. · Organic Letters · 53
Tryptoline-3-hydroxypyridinaldoxime conjugates as efficient reactivators of phosphylated human acetyl and butyrylcholinesterases
2014 · Julien Renou, Mélanie Loiodice, et al. · Chemical Communications · 51
Regioselective de-O-benzylation of monosaccharides
2002 · J.R. Falck, D.K. Barma, et al. · Tetrahedron Letters · 51
Theoretical Mechanistic Study of the TBD-Catalyzed Intramolecular Aldol Reaction of Ketoaldehydes
2010 · Peter Hammar, Cynthia Ghobril, et al. · The Journal of Organic Chemistry · 49
Chromium Vinylidene Carbenoids: Generation, Characterization, and Reactivity. First Evidence for an Internal Proton Return Phenomenon with Vinylidene Carbenoids
2001 · Rachid Baati, D. K. Barma, et al. · Journal of the American Chemical Society · 49
Improved non-covalent biofunctionalization of multi-walled carbon nanotubes using carbohydrate amphiphiles with a butterfly-like polyaromatic tail
2010 · Mohyeddin Assali, Manuel Pernía Leal, et al. · Nano Research · 48
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Semi‐Covalent Surface Molecular Imprinting of Polymers by One‐Stage Mini‐emulsion Polymerization: Glucopyranoside as a Model Analyte
2009 · Pasquale Curcio, Christelle Zandanel, et al. · Macromolecular Bioscience · 48
Tailoring carbon nanotube surfaces with glyconanorings: new bionanomaterials with specific lectin affinity
2009 · Noureddine Khiar, Manuel Pernia Leal, et al. · Chemical Communications · 46
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The risk associated with organophosphorus nerve agents: from their discovery to their unavoidable threat, current medical countermeasures and perspectives
2024 · Camille Voros, José Dias, et al. · Chemico-Biological Interactions · 45
Stereoselective Transformations of Trihalomethylcarbinols Induced by Chromous Chloride
2005 · Romain Bejot, Steve Tisserand, et al. · Angewandte Chemie International Edition · 45
Works count: 171
Citation count: 3,070
H-index: 32
I10-index: 71
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