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 alpha-SeCF3 substituted carbonyl derivatives using an in situ generated electrophilic ClSeCF3 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 / E. Massolo, M. Pirola, S. Rossi, T. Benincori. - In: MOLECULES. - ISSN 1420-3049. - 24:4(2019 Feb 18), pp. 726.1-726.8. [10.3390/molecules24040726]

Metal-Free Alpha Trifluoromethylselenolation of Carbonyl Derivatives under Batch and Flow Conditions

Massolo, Elisabetta;Pirola, Margherita;Rossi, Sergio;
2019-02-18

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 alpha-SeCF3 substituted carbonyl derivatives using an in situ generated electrophilic ClSeCF3 species. We also implemented an in-flow protocol to improve the safety features of the process.
trifluoromethylselenolation; carbonyl compounds; selenium; fluorinated derivatives; flow chemistry
Settore CHIM/06 - Chimica Organica
MOLECULES
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/626370
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