The direct borylation of disubstituted alkenes is reported. These conditions allow for the conversion of a variety 1,1- and 1,2-disubstituted alkenes to trisubstituted alkenyl boronic esters with outstanding yields and excellent E/Z selectivities. The utility of this reaction has been demonstrated with several downstream functionalization reactions, which allow access to diverse, stereodefined, functionalized olefins. Mechanistic studies are consistent with a boryl-Heck pathway
An efficient approach to tetrasubstituted alkenylboronates via a cascade borylation/B–O elimination ...
New alkenylboronic esters were synthesised from halo-substituted alkenylboronic esters through cross...
The synthesis of organoboron compounds have attracted the attention of the synthetic community. In p...
Reported herein is the efficient synthesis of tetra- and tri-substituted ( Z )-fluoro- and ( Z )-chl...
Transition-metal catalyzed cross-coupling has, in many ways, revolutionized synthetic chemistry by p...
A variety of terminal alkenes, as well as heteroaromatic compounds, are borylated by the combined us...
Watson, Donald A.Unsaturated heteroatomic compounds are an important class of molecules in many disc...
The copper-catalyzed diboration of ketones followed by an acid-catalyzed elimination leads to the fo...
Polyborylated-alkenes are valuable reagents in modern organic synthesis, providing access to a wide ...
Palladium catalyzed allylic C-H functionalization was performed using exocyclic alkene substrates. M...
A highly regio- and stereoselective silylborylation of an alkynylboronate is disclosed. PhMe<sub>2</...
A highly regio- and stereoselective silylborylation of an alkynylboronate is disclosed. PhMe<sub>2</...
Organoboron compounds and borylated heterocycles are in general versatile building blocks and precur...
Organoboron compounds and borylated heterocycles are in general versatile building blocks and precur...
A highly regio- and stereoselective silylborylation of an alkynylboronate is disclosed. PhMe<sub>2</...
An efficient approach to tetrasubstituted alkenylboronates via a cascade borylation/B–O elimination ...
New alkenylboronic esters were synthesised from halo-substituted alkenylboronic esters through cross...
The synthesis of organoboron compounds have attracted the attention of the synthetic community. In p...
Reported herein is the efficient synthesis of tetra- and tri-substituted ( Z )-fluoro- and ( Z )-chl...
Transition-metal catalyzed cross-coupling has, in many ways, revolutionized synthetic chemistry by p...
A variety of terminal alkenes, as well as heteroaromatic compounds, are borylated by the combined us...
Watson, Donald A.Unsaturated heteroatomic compounds are an important class of molecules in many disc...
The copper-catalyzed diboration of ketones followed by an acid-catalyzed elimination leads to the fo...
Polyborylated-alkenes are valuable reagents in modern organic synthesis, providing access to a wide ...
Palladium catalyzed allylic C-H functionalization was performed using exocyclic alkene substrates. M...
A highly regio- and stereoselective silylborylation of an alkynylboronate is disclosed. PhMe<sub>2</...
A highly regio- and stereoselective silylborylation of an alkynylboronate is disclosed. PhMe<sub>2</...
Organoboron compounds and borylated heterocycles are in general versatile building blocks and precur...
Organoboron compounds and borylated heterocycles are in general versatile building blocks and precur...
A highly regio- and stereoselective silylborylation of an alkynylboronate is disclosed. PhMe<sub>2</...
An efficient approach to tetrasubstituted alkenylboronates via a cascade borylation/B–O elimination ...
New alkenylboronic esters were synthesised from halo-substituted alkenylboronic esters through cross...
The synthesis of organoboron compounds have attracted the attention of the synthetic community. In p...