857934-89-5

Upstream product

• 100-52-7 benzaldehyde 
• 594823-67-3 (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)bromobenzene) 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 1195-66-0 2-methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 89598-96-9 (3-bromophenyl)boronic acid 
• 408492-28-4 2-(3-iodo-phenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane 

Relevant academic research and scientific papers

Use of in situ isopropoxide protection in the metal-halogen exchange of arylboronates

(Chemical Equation Presented) Isopropoxide protection of arylboronates allowed their use in metal-halogen exchange reactions. The isopropoxide- protected borate species were obtained from a boronate or in situ from dibromoarenes. meta- and para-dibromoare

Preparation and selective reactions of mixed bimetallic aromatic and heteroaromatic boron-magnesium reagents

(Chemical Equation Presented) It's all in the mix: The magnesiation of iodoaryl and iodoheteroaryl boronic esters with iPrMgCl·LiCl leads to mixed bimetallic compounds, which react with a variety of electrophiles to provide highly functionalized boronic e