2,4-Bis(Fluoroalkyl)
2,4-Bis(fluoroalkyl)quinoline-3-carboxylates as Tools for the Development of Potential Agrochemical Ingredients Fallia Aribi, Armen Panossian, Jean-Pierre Vors, Sergiy Pazenok, Frédéric Leroux To cite this version: Fallia Aribi, Armen Panossian, Jean-Pierre Vors, Sergiy Pazenok, Frédéric Leroux. 2,4- Bis(fluoroalkyl)quinoline-3-carboxylates as Tools for the Development of Potential Agrochemical Ingre- dients. European Journal of Organic Chemistry, Wiley-VCH Verlag, 2018, Organofluorine Chemistry in Europe, 2018 (27-28), pp.3792-3802. 10.1002/ejoc.201800375. hal-02105501 HAL Id: hal-02105501 https://hal.archives-ouvertes.fr/hal-02105501 Submitted on 13 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 2,4-Bis(fluoroalkyl)quinoline-3-carboxylates as tools for the development of potential agrochemical ingredients Fallia Aribi,[a,b] Armen Panossian,[a,b] Jean-Pierre Vors,[b,c] Sergii Pazenok,[b,d] and Frédéric R. Leroux*[a,b] Abstract: From an easy and scalable synthetic access to quinoline groups appended to heteroaromatics may enhance the derivatives substituted by fluorinated groups in both C2- and C4- lipophilicity and oxidative stability of bioactive molecules.[5] positions developed in our laboratory, we devised the synthesis of a Despite this interest, only few series of quinolines substituted in new series of unprecedented 2,4-bis(fluoroalkyl)quinoline-3- C2- and C4-positions by fluorinated groups have been reported,[3c, carboxylates in two steps only.
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