{"date_published":"2022-07-17T00:00:00Z","publisher":"American Chemical Society","year":"2022","article_type":"original","day":"17","intvolume":"        24","language":[{"iso":"eng"}],"issue":"29","oa_version":"Published Version","main_file_link":[{"open_access":"1","url":"https://doi.org/10.26434/chemrxiv-2022-mstv5"}],"quality_controlled":"1","scopus_import":"1","title":"Benzylic fluorination induced by a charge-transfer complex with a solvent-dependent selectivity switch","citation":{"chicago":"Madani, Amiera, Lucia Anghileri, Matthias Heydenreich, Heiko M. Möller, and Bartholomäus Pieber. “Benzylic Fluorination Induced by a Charge-Transfer Complex with a Solvent-Dependent Selectivity Switch.” <i>Organic Letters</i>. American Chemical Society, 2022. <a href=\"https://doi.org/10.1021/acs.orglett.2c02050\">https://doi.org/10.1021/acs.orglett.2c02050</a>.","ista":"Madani A, Anghileri L, Heydenreich M, Möller HM, Pieber B. 2022. Benzylic fluorination induced by a charge-transfer complex with a solvent-dependent selectivity switch. Organic Letters. 24(29), 5376–5380.","apa":"Madani, A., Anghileri, L., Heydenreich, M., Möller, H. M., &#38; Pieber, B. (2022). Benzylic fluorination induced by a charge-transfer complex with a solvent-dependent selectivity switch. <i>Organic Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.orglett.2c02050\">https://doi.org/10.1021/acs.orglett.2c02050</a>","short":"A. Madani, L. Anghileri, M. Heydenreich, H.M. Möller, B. Pieber, Organic Letters 24 (2022) 5376–5380.","ama":"Madani A, Anghileri L, Heydenreich M, Möller HM, Pieber B. Benzylic fluorination induced by a charge-transfer complex with a solvent-dependent selectivity switch. <i>Organic Letters</i>. 2022;24(29):5376–5380. doi:<a href=\"https://doi.org/10.1021/acs.orglett.2c02050\">10.1021/acs.orglett.2c02050</a>","mla":"Madani, Amiera, et al. “Benzylic Fluorination Induced by a Charge-Transfer Complex with a Solvent-Dependent Selectivity Switch.” <i>Organic Letters</i>, vol. 24, no. 29, American Chemical Society, 2022, pp. 5376–5380, doi:<a href=\"https://doi.org/10.1021/acs.orglett.2c02050\">10.1021/acs.orglett.2c02050</a>.","ieee":"A. Madani, L. Anghileri, M. Heydenreich, H. M. Möller, and B. Pieber, “Benzylic fluorination induced by a charge-transfer complex with a solvent-dependent selectivity switch,” <i>Organic Letters</i>, vol. 24, no. 29. American Chemical Society, pp. 5376–5380, 2022."},"month":"07","date_created":"2022-09-08T11:34:30Z","article_processing_charge":"No","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa":1,"status":"public","page":"5376–5380","publication_identifier":{"issn":["1523-7060"],"eissn":["1523-7052"]},"date_updated":"2023-05-08T08:39:34Z","volume":24,"extern":"1","type":"journal_article","publication":"Organic Letters","publication_status":"published","abstract":[{"text":"We present a divergent strategy for the fluorination of phenylacetic acid derivatives that is induced by a charge-transfer complex between Selectfluor and 4-(dimethylamino)pyridine. A comprehensive investigation of the conditions revealed a critical role of the solvent on the reaction outcome. In the presence of water, decarboxylative fluorination through a single-electron oxidation is dominant. Non-aqueous conditions result in the clean formation of α-fluoro-α-arylcarboxylic acids.","lang":"eng"}],"_id":"12067","doi":"10.1021/acs.orglett.2c02050","author":[{"first_name":"Amiera","full_name":"Madani, Amiera","last_name":"Madani"},{"last_name":"Anghileri","full_name":"Anghileri, Lucia","first_name":"Lucia"},{"first_name":"Matthias","full_name":"Heydenreich, Matthias","last_name":"Heydenreich"},{"full_name":"Möller, Heiko M.","first_name":"Heiko M.","last_name":"Möller"},{"orcid":"0000-0001-8689-388X","full_name":"Pieber, Bartholomäus","first_name":"Bartholomäus","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","last_name":"Pieber"}]}