The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free approach using arynes has been developed. The reaction afforded functionalized diaryl amines in moderate to excellent yield. High levels of functional group compatibility especially with halogen containing substrates, dyes and donor–acceptor systems, and high yields of products are the notable features of the present reaction
Arynes are employed in the transition-metal-free and mild [2,3] Stevens rearrangement of tertiary al...
Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate f...
The transition-metal-free multicomponent coupling involving arynes, aromatic tertiary amines, and CO...
A transition metal-free N-arylation of primary and secondary amines with diaryliodonium salts is pre...
The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and...
A facile, fluoride-induced transition-metal-free chemoselective α-arylation of β-dicarbonyl compound...
A rapid, transition metal-free, high-yielding, tetrabutylammonium bromide-promoted method of N-aryla...
A simple and reliable reaction protocol for the clean, fast, and high-yielding synthesis of various ...
Since the word “organocatalysis” has been created by MacMillan in 2000, it has growing very fast and...
With a strategy of the formation of benzynes by using diaryliodonium salts, a cycloaddition reaction...
A new palladium-catalyzed free-amine directed arylation of C(sp<sup>2</sup>)–H bonds in the presence...
The transition-metal-free multicomponent coupling of arynes, aromatic tertiary amines, and aldehydes...
Direct preparation of tertiary amines in which two substituents are aromatic is described. In the pr...
This thesis describes new approaches to achieve efficient and selective (hetero)arene derivatization...
A mild and metal-free approach to C−N coupling is described that employs diaryliodonium salt electro...
Arynes are employed in the transition-metal-free and mild [2,3] Stevens rearrangement of tertiary al...
Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate f...
The transition-metal-free multicomponent coupling involving arynes, aromatic tertiary amines, and CO...
A transition metal-free N-arylation of primary and secondary amines with diaryliodonium salts is pre...
The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and...
A facile, fluoride-induced transition-metal-free chemoselective α-arylation of β-dicarbonyl compound...
A rapid, transition metal-free, high-yielding, tetrabutylammonium bromide-promoted method of N-aryla...
A simple and reliable reaction protocol for the clean, fast, and high-yielding synthesis of various ...
Since the word “organocatalysis” has been created by MacMillan in 2000, it has growing very fast and...
With a strategy of the formation of benzynes by using diaryliodonium salts, a cycloaddition reaction...
A new palladium-catalyzed free-amine directed arylation of C(sp<sup>2</sup>)–H bonds in the presence...
The transition-metal-free multicomponent coupling of arynes, aromatic tertiary amines, and aldehydes...
Direct preparation of tertiary amines in which two substituents are aromatic is described. In the pr...
This thesis describes new approaches to achieve efficient and selective (hetero)arene derivatization...
A mild and metal-free approach to C−N coupling is described that employs diaryliodonium salt electro...
Arynes are employed in the transition-metal-free and mild [2,3] Stevens rearrangement of tertiary al...
Herein, we report a transition-metal-free annulation reaction of benzynes and 1,3-oxopentanedioate f...
The transition-metal-free multicomponent coupling involving arynes, aromatic tertiary amines, and CO...