A method for conducting selenium-promoted intermolecular Friedel–Crafts (F–C) alkylation reactions has been developed with simple alkenes using trimethylsilyl trifluoromethanesulfonate as a catalyst and <i>N</i>-phenylselenophthalimide as an efficient selenium source. Electron-rich arenes smoothly underwent F–C alkylation with a variety of alkenes to afford alkylated products in good yield and with high regioselectivity and diastereoselectivity. The regioselectivity and stereoselectivity of arenes and alkenes as well as a preliminary mechanism of the F–C alkylation reaction are discussed
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
An enantioselective selenolactonization of olefinic acids has been developed using (DHQD)<sub>2</sub...
By employing cheap and biodegradable natural deep eutectic solvent as the catalyst and reaction medi...
A method for conducting selenium-promoted intermolecular Friedel–Crafts (F–C) alkylation reactions h...
A method for the simple, efficient, and atom-economic amidoselenenylation of simple alkenes under mi...
Chiral selenide-catalyzed oxytrifluoromethylthiolation of aliphatic internal alkenes by a formally i...
A simple procedure for the synthesis of alkyl styryl selenides was developed. This methodology invol...
New chiral diselenides were prepared in a few steps from readily available starting materials. The s...
An efficient approach to vicinal trifluoromethylthioamination of alkenes with a broad substrate scop...
The one-pot efficient synthesis of novel functionalized organoselenium compound by bis-alkoxyselenen...
The first part of this dissertation serves as an introduction to the current state of electrophilic ...
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
Silver(I) catalyzed phenylselenylation of terminal alkynes and organoboronic acids has been demonstr...
A simple and highly chemo- and regioselective method for introducing primary alkyl substituents into...
We report here a method of direct Friedel–Crafts benzylation of arenes with benzylic alcohols using ...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
An enantioselective selenolactonization of olefinic acids has been developed using (DHQD)<sub>2</sub...
By employing cheap and biodegradable natural deep eutectic solvent as the catalyst and reaction medi...
A method for conducting selenium-promoted intermolecular Friedel–Crafts (F–C) alkylation reactions h...
A method for the simple, efficient, and atom-economic amidoselenenylation of simple alkenes under mi...
Chiral selenide-catalyzed oxytrifluoromethylthiolation of aliphatic internal alkenes by a formally i...
A simple procedure for the synthesis of alkyl styryl selenides was developed. This methodology invol...
New chiral diselenides were prepared in a few steps from readily available starting materials. The s...
An efficient approach to vicinal trifluoromethylthioamination of alkenes with a broad substrate scop...
The one-pot efficient synthesis of novel functionalized organoselenium compound by bis-alkoxyselenen...
The first part of this dissertation serves as an introduction to the current state of electrophilic ...
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
Silver(I) catalyzed phenylselenylation of terminal alkynes and organoboronic acids has been demonstr...
A simple and highly chemo- and regioselective method for introducing primary alkyl substituents into...
We report here a method of direct Friedel–Crafts benzylation of arenes with benzylic alcohols using ...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
An enantioselective selenolactonization of olefinic acids has been developed using (DHQD)<sub>2</sub...
By employing cheap and biodegradable natural deep eutectic solvent as the catalyst and reaction medi...