Trifluoromethylselenolated carbonyl compounds represent an emerging class with potential applications in several fields; however, a widespread use of such compound is hampered by the very limited number of strategies for their preparation. In this study we developed a method for the preparation of α-SeCF 3 substituted carbonyl derivatives using an in situ generated electrophilic ClSeCF 3 species. We also implemented an in-flow protocol to improve the safety features of the process.

Metal-free alpha trifluoromethylselenolation of carbonyl derivatives under batch and flow conditions

Benincori, Tiziana
2019-01-01

Abstract

Trifluoromethylselenolated carbonyl compounds represent an emerging class with potential applications in several fields; however, a widespread use of such compound is hampered by the very limited number of strategies for their preparation. In this study we developed a method for the preparation of α-SeCF 3 substituted carbonyl derivatives using an in situ generated electrophilic ClSeCF 3 species. We also implemented an in-flow protocol to improve the safety features of the process.
2019
https://www.mdpi.com/1420-3049/24/4/726/pdf
Carbonyl compounds; Flow chemistry; Fluorinated derivatives; Selenium; Trifluoromethylselenolation; Analytical Chemistry; Chemistry (miscellaneous); Molecular Medicine; 3003; Drug Discovery3003 Pharmaceutical Science; Physical and Theoretical Chemistry; Organic Chemistry
Massolo, Elisabetta; Pirola, Margherita; Rossi, Sergio; Benincori, Tiziana
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/2077486
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