Regioselective halogenation of arenes and heterocycles with <i>N</i>-halosuccinimides in fluorinated alcohols is disclosed. Under mild condition reactions, a wide diversity of halogenated arenes are obtained in good yields with high regioselectivity. Additionally, the versatility of the method is demonstrated by the development of one-pot sequential halogenation and halogenation-Suzuki cross-coupling reactions
The purpose of this work is the synthesis and design of new ways of functionalization of some fluori...
Functionalized per- and polyfluoroarenes are important building blocks, with many industrially and m...
Vicinal halofluorides have been prepared from the corresponding alkenes by reaction with a stoicheio...
We report an efficient method for the regiodivergent synthesis of halogenated resorcinol derivatives...
In view of the expanding interest in fluorinated heterocycles, the installation of a fluoroalkyl gro...
A simple, rapid and highly regioselective green protocol has been developed for the halogenation of ...
The organometallic approach to the functionalization of arenes and heteroarenes has recently been in...
A new method of brominating aromatic and heteroaromatic ring systems is investigated. The combinati...
Stereoselective additions of highly functionalized reagents to available unsaturated hydrocarbons ar...
The Brønsted-Acidic ionic liquid 1-methyl-3-(4-sulfobutyl) imidazolium triflate [BMIM(SO3H)][OTf] wa...
Gas-phase techniques were used to examine the halogenation of deprotonated heterocycles by perfluoro...
Methods to functionalize arenes and heteroarenes in a site-selective manner are highly sought after ...
A mild phosphine sulfide catalyzed electrophilic halogenation of arenes and heterocycles that utiliz...
Due to the electron-withdrawing character of fluoroalkyl groups, fluorinated alcohols such as triflu...
Oxygen and nitrogen heterocycles are well-known classes of compounds due to their excellent biologic...
The purpose of this work is the synthesis and design of new ways of functionalization of some fluori...
Functionalized per- and polyfluoroarenes are important building blocks, with many industrially and m...
Vicinal halofluorides have been prepared from the corresponding alkenes by reaction with a stoicheio...
We report an efficient method for the regiodivergent synthesis of halogenated resorcinol derivatives...
In view of the expanding interest in fluorinated heterocycles, the installation of a fluoroalkyl gro...
A simple, rapid and highly regioselective green protocol has been developed for the halogenation of ...
The organometallic approach to the functionalization of arenes and heteroarenes has recently been in...
A new method of brominating aromatic and heteroaromatic ring systems is investigated. The combinati...
Stereoselective additions of highly functionalized reagents to available unsaturated hydrocarbons ar...
The Brønsted-Acidic ionic liquid 1-methyl-3-(4-sulfobutyl) imidazolium triflate [BMIM(SO3H)][OTf] wa...
Gas-phase techniques were used to examine the halogenation of deprotonated heterocycles by perfluoro...
Methods to functionalize arenes and heteroarenes in a site-selective manner are highly sought after ...
A mild phosphine sulfide catalyzed electrophilic halogenation of arenes and heterocycles that utiliz...
Due to the electron-withdrawing character of fluoroalkyl groups, fluorinated alcohols such as triflu...
Oxygen and nitrogen heterocycles are well-known classes of compounds due to their excellent biologic...
The purpose of this work is the synthesis and design of new ways of functionalization of some fluori...
Functionalized per- and polyfluoroarenes are important building blocks, with many industrially and m...
Vicinal halofluorides have been prepared from the corresponding alkenes by reaction with a stoicheio...