This study describes the solid-state palladium-catalyzed cross-coupling between aryl halides and bis(pinacolato)diboron using ball milling. The reactions were completed within 10 min for most aryl halides to afford a variety of synthetically useful arylboronates in high yields. Notably, all experimental operations could be performed in air, and did not require the use of large amounts of dry and degassed organic solvents. The utility of this method was further demonstrated by gram-scale synthesis under solvent-free, mechanochemical conditions
Organic reactions that employ moisture- and/or oxygen-sensitive reagents or intermediates usually in...
Sonogashira coupling represents an indispensable tool for the preparation of organic materials that ...
Chemical vapor deposition (CVD) precursor chemicals are held to some of the highest purity levels in...
The Suzuki-Miyaura cross-coupling between poly-fluorinated arylboron nucleophiles and aryl halides e...
Mechanochemistry has been applied for the first time to an iridium(I)-catalyzed C-H borylation react...
Abstract A facile and efficient palladium-catalyzed borylation of aryl (pseudo)halides at room tempe...
The molecular Suzuki cross-coupling reaction was conducted mechanochemically, with neither solvents,...
Although much current research focuses on developing new boron reagents and identifying robust catal...
The combination of Pd(dba)_2 and bis(2-di-tert-butylphosphinophenyl)ether has proven to be efficient...
ABSTRACT PALLADIUM-CATALYZED BORYLATION AND CROSS-COUPLING OF ARYL AND HETEROARYL HALIDES UTILIZING ...
The milling ball is the catalyst. We introduce a palladium‐catalyzed reaction inside a ball mill, wh...
Abstract: Tetrakis(alkoxo)diborons cross-coupled with aryl triflates at 80 。C in the presence of PdC...
Within this thesis is described a series of studies into performing organic synthesis under mechanoc...
A fast and site-selective biaryl synthesis via dehydrogenative C–H/C–H arylation in a ball mill was ...
A metal-free synthetic method for arylboronic pinacol esters from easily available aromatic amines a...
Organic reactions that employ moisture- and/or oxygen-sensitive reagents or intermediates usually in...
Sonogashira coupling represents an indispensable tool for the preparation of organic materials that ...
Chemical vapor deposition (CVD) precursor chemicals are held to some of the highest purity levels in...
The Suzuki-Miyaura cross-coupling between poly-fluorinated arylboron nucleophiles and aryl halides e...
Mechanochemistry has been applied for the first time to an iridium(I)-catalyzed C-H borylation react...
Abstract A facile and efficient palladium-catalyzed borylation of aryl (pseudo)halides at room tempe...
The molecular Suzuki cross-coupling reaction was conducted mechanochemically, with neither solvents,...
Although much current research focuses on developing new boron reagents and identifying robust catal...
The combination of Pd(dba)_2 and bis(2-di-tert-butylphosphinophenyl)ether has proven to be efficient...
ABSTRACT PALLADIUM-CATALYZED BORYLATION AND CROSS-COUPLING OF ARYL AND HETEROARYL HALIDES UTILIZING ...
The milling ball is the catalyst. We introduce a palladium‐catalyzed reaction inside a ball mill, wh...
Abstract: Tetrakis(alkoxo)diborons cross-coupled with aryl triflates at 80 。C in the presence of PdC...
Within this thesis is described a series of studies into performing organic synthesis under mechanoc...
A fast and site-selective biaryl synthesis via dehydrogenative C–H/C–H arylation in a ball mill was ...
A metal-free synthetic method for arylboronic pinacol esters from easily available aromatic amines a...
Organic reactions that employ moisture- and/or oxygen-sensitive reagents or intermediates usually in...
Sonogashira coupling represents an indispensable tool for the preparation of organic materials that ...
Chemical vapor deposition (CVD) precursor chemicals are held to some of the highest purity levels in...