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Molecules (Basel, Switzerland)|April 3, 2021
Insights into the Mechanism and Catalysis of Peptide Thioester Synthesis by Alkylselenols Provide a New Tool for Chemical Protein SynthesisFlorent Kerdraon, Gemma Bogard, Benoît Snella, et al.Nature Communications|May 24, 2020
A cysteine selenosulfide redox switch for protein chemical synthesisVincent Diemer, Nathalie Ollivier, Bérénice Leclercq, et al.Angewandte Chemie (International Ed. in English)|May 13, 2022
Fast Protein Modification in the Nanomolar Concentration Range Using an Oxalyl Amide as Latent ThioesterBenoît Snella, Benjamin Grain, Jérôme Vicogne, et al.Bioorganic & Medicinal Chemistry|July 28, 2006
Loss of antagonistic activity of tamoxifen by replacement of one N-methyl of its side chain by fluorinated residuesVangelis Agouridas, Ioanna Laïos, Anny Cleeren, et al.Chemical Reviews|May 4, 2019
Native Chemical Ligation and Extended Methods: Mechanisms, Catalysis, Scope, and LimitationsVangelis Agouridas, Ouafâa El Mahdi, Vincent Diemer, et al.The Journal of Organic Chemistry|September 20, 2018
Catalysis of Thiol-Thioester Exchange by Water-Soluble Alkyldiselenols Applied to the Synthesis of Peptide Thioesters and SEA-Mediated LigationMarine Cargoët, Vincent Diemer, Benoît Snella, et al.Journal of Medicinal Chemistry|January 13, 2009
Effect of fluorination on the pharmacological profile of 11beta isomers of fulvestrant in breast carcinoma cellsVangelis Agouridas, Emmanuel Magnier, Jean-Claude Blazejewski, et al.STAR Protocols|October 16, 2024
Protocol for protein modification using oxalyl thioester-mediated chemoselective ligationFrancesco Terzani, Chen Wang, Simindokht Rostami, et al.Pageof 3