A fast and site-selective biaryl synthesis via dehydrogenative C–H/C–H arylation in a ball mill was developed. In this paper, both electron-deficient oximes and electron-rich anilides quickly and under mild conditions provided arylation with various arenes to give the biaryl products in high-level selectivity. Given the solventless mechanochemical conditions, the transformation obviated the use of large amounts of arene coupling partners as solvents and allowed utilization of more-complicated and more-expensive arenes as coupling partners, which may dramatically enhance the application prospect of the C–H/C–H arylation strategy
A striking breakthrough to the frame of traditional cross-couplings/C-H functionalizations using an ...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
Solvent-free reaction using a high-speed ball milling technique has been applied to the classical Ul...
NoMechanochemistry enabled the selective synthesis of the recherche´ orange polymorph of Wilkinson’...
Hydrogenation and dehydrogenation reactions are one of the pillars of the chemical industry, with ap...
This study describes the solid-state palladium-catalyzed cross-coupling between aryl halides and bis...
Mechanochemical ball milling catalytic transfer hydrogenation (CTH) of aromatic nitro compounds usin...
<div><p></p><p>We report here a simple, efficient, and environmentally friendly methodology for elec...
This thesis deals with the development of novel mechanochemical-induced C-H functionalizations in ba...
Mechanochemistry involves milling reagents in a ball mill to induce reaction. Typically, mechanochem...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
Mechanochemical synthesis, as used in this work, is the mechanical milling of reagents to drive reac...
Recognizing the need for efficient routes to biaryl compounds, chemists have developed an arsenal of...
Mechanochemistry has been applied for the first time to an iridium(I)-catalyzed C-H borylation react...
Bi(NO3)3·5H2O/MgSO4 was developed as an efficient and green reagent for the nitration of aromatic co...
A striking breakthrough to the frame of traditional cross-couplings/C-H functionalizations using an ...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
Solvent-free reaction using a high-speed ball milling technique has been applied to the classical Ul...
NoMechanochemistry enabled the selective synthesis of the recherche´ orange polymorph of Wilkinson’...
Hydrogenation and dehydrogenation reactions are one of the pillars of the chemical industry, with ap...
This study describes the solid-state palladium-catalyzed cross-coupling between aryl halides and bis...
Mechanochemical ball milling catalytic transfer hydrogenation (CTH) of aromatic nitro compounds usin...
<div><p></p><p>We report here a simple, efficient, and environmentally friendly methodology for elec...
This thesis deals with the development of novel mechanochemical-induced C-H functionalizations in ba...
Mechanochemistry involves milling reagents in a ball mill to induce reaction. Typically, mechanochem...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
Mechanochemical synthesis, as used in this work, is the mechanical milling of reagents to drive reac...
Recognizing the need for efficient routes to biaryl compounds, chemists have developed an arsenal of...
Mechanochemistry has been applied for the first time to an iridium(I)-catalyzed C-H borylation react...
Bi(NO3)3·5H2O/MgSO4 was developed as an efficient and green reagent for the nitration of aromatic co...
A striking breakthrough to the frame of traditional cross-couplings/C-H functionalizations using an ...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
Solvent-free reaction using a high-speed ball milling technique has been applied to the classical Ul...