A method for transition metal-free 1,2-carboboration of unactivated alkenes with bis(catecholato)diboron as the boron source in combination with alkyl halides as the alkyl component is introduced. The three-component reaction proceeds via a radical pathway on a broad range of unactivated alkenes, and the 1,2-carboboration products serve as valuable synthetic building blocks. Density functional theory calculations provide insights into the mechanism
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A 1,3,4-trisubstituted borole is readily obtained by a 1,1-carboboration sequence starting from a bi...
A 1,3,4-trisubstituted borole is readily obtained by a 1,1-carboboration sequence starting from a bi...
During the past decade, many research groups have described catalytic methods for 1,2‐carboboration,...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
This work explains the reactivity of diboron reagents with 1,3-dienes in a transition-metal-free con...
The transition-metal-free intermolecular direct 1,2-carboboration reaction of heteroarylacetylenes u...
1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-func...
1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-func...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
We report the first transition metal-free and <i>trans</i>-selective alkynylboration reaction of alk...
We reveal here the regioselective nucleophilic addition of C(sp3) to 1,1-arylboryl alkenes, followed...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
We report the first transition metal-free and <i>trans</i>-selective alkynylboration reaction of alk...
AbstractCatalyst‐free 1,2‐carboboration of ynamides is presented. Readily available aryldichlorobora...
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A 1,3,4-trisubstituted borole is readily obtained by a 1,1-carboboration sequence starting from a bi...
A 1,3,4-trisubstituted borole is readily obtained by a 1,1-carboboration sequence starting from a bi...
During the past decade, many research groups have described catalytic methods for 1,2‐carboboration,...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
This work explains the reactivity of diboron reagents with 1,3-dienes in a transition-metal-free con...
The transition-metal-free intermolecular direct 1,2-carboboration reaction of heteroarylacetylenes u...
1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-func...
1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-func...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
We report the first transition metal-free and <i>trans</i>-selective alkynylboration reaction of alk...
We reveal here the regioselective nucleophilic addition of C(sp3) to 1,1-arylboryl alkenes, followed...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
We report the first transition metal-free and <i>trans</i>-selective alkynylboration reaction of alk...
AbstractCatalyst‐free 1,2‐carboboration of ynamides is presented. Readily available aryldichlorobora...
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A 1,3,4-trisubstituted borole is readily obtained by a 1,1-carboboration sequence starting from a bi...
A 1,3,4-trisubstituted borole is readily obtained by a 1,1-carboboration sequence starting from a bi...