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Synthetic Approaches to Trifluoromethylselenolated Compounds
Author(s) -
Tlili Anis,
Ismalaj Ermal,
Glenadel Quentin,
Ghiazza Clément,
Billard Thierry
Publication year - 2018
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201704637
Subject(s) - lipophilicity , chalcogen , trifluoromethyl , chemistry , group (periodic table) , organic chemistry , combinatorial chemistry , alkyl
The association of trifluoromethyl group to chalcogens gives new fluorinated substituents with specific properties, mainly in term of lipophilicity. The trifluoromethylselenyl group is the last of the series that has been studied and despite pioneering approaches in the late 1960s, CF 3 Se chemistry has been scarcely developed over the last decades. Some modern and efficient methods to obtain trifluoromethylselenolated molecules have recently emerged. This Review describes the advancements that have been reported.