916658-73-6

Upstream product

• 73183-34-3 bis(pinacol)diborane 
• 98-83-9 isopropenylbenzene 
• 78782-27-1 4,4,5,5-tetramethyl-2-styryl-[1,3,2]dioxaborolane 
• 51075-23-1 trimethyl((2-phenylprop-1-en-1-yl)oxy)silane 
• 1377151-56-8 4,4,5,5-tetramethyl-2-{2-[4-(trifluoromethyl)phenyl]ethenyl}-1,3,2-dioxaborolane 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Downstream Products

• 14037-02-6 2-(2-phenyl-propenyl)-pyridine 
• 257299-03-9 (R)-(+)-4,4,5,5-tetramethyl-2-(2-phenylpropyl)-1,3,2-dioxaborolane 

Relevant academic research and scientific papers

Alkenyl boron compound and preparation method and application thereof

The invention discloses an alkenyl boron compound and a preparation method and application thereof. The preparation method comprises the following steps: in a protective atmosphere, enabling a uniformly mixed reaction system containing a lithium enol reag

Method for synthesizing alkenyl borate compound through transfer boronation

The invention relates to a method for synthesizing an alkenyl borate compound by a transfer boronation. The method comprises the steps that substituted olefin and styrene boronic acid pinacol ester are dissolved into a solvent, then a zirconium catalyst i

Synthetic method of alkenyl borate compound

The invention relates to a synthesis method of an alkenyl borate compound, which comprises the following steps: dissolving an olefin compound and a borane compound in a solvent, adding a zirconium catalyst, reacting at 0-150 DEG C for 5 minutes to 8 hours

Selective Dehydrogenative Mono- or Diborylation of Styrenes by Supported Copper Catalysts

The selective dehydrogenative borylation of alkenes is an attractive method for synthesizing useful borylalkenes. However, very few catalytic systems have been reported that fulfill this objective. All the reported examples are homogeneous catalysts with

Dehydrogenative Borylation and Silylation of Styrenes Catalyzed by Copper-Carbenes

Readily available copper precatalysts, (NHC)CuOtBu (NHC = N-heterocyclic carbene), catalyze dehydrogenative borylation and silylation of styrenes with moderate to high yields, using ketone additives as sacrificial oxidants. This method provides access to

Rhodium-catalyzed dehydrogenative borylation of cyclic alkenes

A rhodium-catalyzed dehydrogenative borylation of cyclic alkenes is described. This reaction provides direct access to cyclic 1-alkenylboronic acid pinacol esters, useful intermediates in organic synthesis. Suzuki-Miyaura cross-coupling applications are also presented. The Royal Society of Chemistry 2010.