Zweifel olefination is a catalyst-free reaction that serves alkene functionalization. While most methods employ commercially available boron pinacol esters, we have assembled a sequence in which the two partners of the formal coupling reaction are installed successively, starting from inexpensive boron alkoxides. The in situ formation of bisorganoborinates was accomplished by consecutive reaction of two different organometallic species. This single-pot procedure represents a great advancement in the generation of organoborinates and their involvement in C–C bond formation
Organoborane compounds are highly used in a huge number of fields, from medicine, in the boron neutr...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
The formation of carbon-carbon double bonds plays an important role in synthetic organic chemistry. ...
The Zweifel olefination is a powerful method for the stereoselective synthesis of alkenes. The react...
Conventional methods carrying out C(sp2)−C(sp2) bond formations are typically mediated by transition...
Conventional methods carrying out C(sp2)−C(sp2) bond formations are typically mediated by transition...
Boron-containing organometallics are unique for the variety of ways in which they can be synthesized...
Boron-containing organometallics are unique for the variety of ways in which they can be synthesized...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
Conventional methods carrying out C(sp2)−C(sp2) bond formations are typically mediated by transition...
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 catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A new transition-metal-free borylation of aryl and vinyl halides using 1,1-bis[(pinacolato)boryl]alk...
Organoborane compounds are highly used in a huge number of fields, from medicine, in the boron neutr...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
The formation of carbon-carbon double bonds plays an important role in synthetic organic chemistry. ...
The Zweifel olefination is a powerful method for the stereoselective synthesis of alkenes. The react...
Conventional methods carrying out C(sp2)−C(sp2) bond formations are typically mediated by transition...
Conventional methods carrying out C(sp2)−C(sp2) bond formations are typically mediated by transition...
Boron-containing organometallics are unique for the variety of ways in which they can be synthesized...
Boron-containing organometallics are unique for the variety of ways in which they can be synthesized...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
Conventional methods carrying out C(sp2)−C(sp2) bond formations are typically mediated by transition...
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 catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A new transition-metal-free borylation of aryl and vinyl halides using 1,1-bis[(pinacolato)boryl]alk...
Organoborane compounds are highly used in a huge number of fields, from medicine, in the boron neutr...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...
Over the years, organoboron species have been vastly utilized in synthetic organic chemistry. Tradit...