A novel, mild, and practical method of amination of simple nonfunctionalized arenes under metal free conditions has been developed. The approach allows coupling of electron-rich arenes with amino derivatives of electron-deficient heterocycles providing rapid access to scaffolds of bioactive compounds and is based on the application of the hypervalent iodine(III) reagent as an oxidant. Regioselective functionalization of C–H bonds of arenes by the formation of C–N bonds under organocatalytic conditions was demonstrated
An oxidative 3-amination of indole derivatives using hypervalent iodine(III) and bissulfonimides, wh...
An advanced protocol for the intramolecular C–H amination of alkyl groups via amidyl radicals (Hofma...
α-Functionalized carbonyl compounds are versatile intermediates in organic synthesis. A broad range ...
An oxidative amination of allenes using a single hypervalent iodine reagent is reported. The reactio...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Five-membered heterocycles are well known for their innate nucleophilicity. In contrast, reaction of...
Novel transition metal-free-mediated amination of C–H bonds with the use of arylsulfonyliminophenyli...
A new approach to direct intermolecular allylic amination has been developed using metal-free condit...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...
In past two decades, hypervalent iodine chemistry has developed as an important tool in synthetic an...
This review summarizes the chemistry of hypervalent iodine(III) compounds with emphasis of their syn...
The synthesis of carbon-nitrogen (C-N) bonds is an area of research that has garnered significant in...
A transition-metal-free, mild, and highly regioselective synthesis of nitroarenes from arenes has be...
Hypervalent iodine reagents are environmentally benign alternatives to heavy metal oxidants. They a...
This review summarizes the chemistry of hypervalent iodine(III) compounds with emphasis of their syn...
An oxidative 3-amination of indole derivatives using hypervalent iodine(III) and bissulfonimides, wh...
An advanced protocol for the intramolecular C–H amination of alkyl groups via amidyl radicals (Hofma...
α-Functionalized carbonyl compounds are versatile intermediates in organic synthesis. A broad range ...
An oxidative amination of allenes using a single hypervalent iodine reagent is reported. The reactio...
Non‐iodinated arenes are easily and selectively converted into (diacetoxyiodo)arenes in a single ste...
Five-membered heterocycles are well known for their innate nucleophilicity. In contrast, reaction of...
Novel transition metal-free-mediated amination of C–H bonds with the use of arylsulfonyliminophenyli...
A new approach to direct intermolecular allylic amination has been developed using metal-free condit...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...
In past two decades, hypervalent iodine chemistry has developed as an important tool in synthetic an...
This review summarizes the chemistry of hypervalent iodine(III) compounds with emphasis of their syn...
The synthesis of carbon-nitrogen (C-N) bonds is an area of research that has garnered significant in...
A transition-metal-free, mild, and highly regioselective synthesis of nitroarenes from arenes has be...
Hypervalent iodine reagents are environmentally benign alternatives to heavy metal oxidants. They a...
This review summarizes the chemistry of hypervalent iodine(III) compounds with emphasis of their syn...
An oxidative 3-amination of indole derivatives using hypervalent iodine(III) and bissulfonimides, wh...
An advanced protocol for the intramolecular C–H amination of alkyl groups via amidyl radicals (Hofma...
α-Functionalized carbonyl compounds are versatile intermediates in organic synthesis. A broad range ...