The development of mild, selective, and practical methods for the introduction of fluorine
atom and fluorine-containing functional groups into organic molecules has received …

The trifluoromethylseleno group (SeCF 3) possesses unique electrosteric effect and high
lipophilicity and has been verified as a pharmaceutically relevant functionality in modulating …

The redox potential gap between arylsulfonium salts and [Me4N][SeCF3] has been clearly
revealed by CV measurements. Construction of the carbon–selenium bond by overcoming …

Herein, we have developed a metal-free, Lewis acid promoted vicinal
oxytrifluoromethylselenolation of alkenes using trifluoromethyl selenoxides as electrophilic …

A visible-light-induced metal-free trifluoromethylselenolation of aryl iodides and bromides
with [Me4N][SeCF3] is described. The reaction was conducted at ambient temperature by …

The trifluoromethylselenyl group (CF3Se) has become an emerging fluorinated moiety in
synthetic chemistry due to its high Hansch lipophilicity parameter and strong electron …

Trifluoromethylselenolation of arenes with [Me4N][SeCF3] in the presence of an oxidant
through Pd-catalyzed C (sp2)–H activation under the assistance of a directing group is …

Due to their high lipophilicity and strong electron‐withdrawing property, more and more
attention has been paid to introducing trifluoromethylseleno and fluoroalkylseleno moieties …

Visible-light-induced decarboxylative trifluoromethylselenolation of (hetero) aromatic
carboxylic acids with [Me4N][SeCF3], oxidant, and catalysts afforded a variety of (hetero) aryl …

Several CF3Se‐substituted α‐amino acid derivatives, such as (R)‐2‐amino‐3‐
((trifluoromethyl) selanyl) propanoates (5 a/6 a),(S)‐2‐amino‐4‐((trifluoromethyl) selanyl) …