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Upstream product

• 210907-84-9 3-aminophenylboronic acid pinacolate 
• 68716-48-3 4,4,5,5-tetramethyl-2-(3-nitrophenyl)-1,3,2-dioxaborolane 
• 73183-34-3 bis(pinacol)diborane 
• 99-09-2 3-nitro-aniline 
• 108-36-1 1,3-dibromobenzene 
• 150255-96-2 (3‐cyanophenyl)boronic acid 

Relevant academic research and scientific papers

Oxazole or thiazole compound and organic electroluminescent device thereof

The invention provides an oxazole or thiazole compound and an organic electroluminescent device thereof. Belong to organic electroluminescence technical field. The oxazole or thiazole compound provided by the invention has a proper HOMO energy level, can

SMALL MOLECULE INHIBITORS OF DIHYDROFOLATE REDUCTASE

The disclosure relates to compositions and methods for the treatment of fungal, bacterial, and parasitic infections and inhibition of fungal, bacterial, and parasitic growth. In particular, such compositions include dihydrofolate reductase (DHFR) inhibito

Synthesis of trimethylstannyl arylboronate compounds by sandmeyer-type transformations and their applications in chemoselective cross-coupling reactions

A synthetic method based on Sandmeyer-type reactions to access both tin- and boron-substituted arenes from nitroaniline derivatives is described. This transformation can be applied to the synthesis of a series of functionalized trimethylstannyl arylboronates. In addition, the chemoselective reaction of the Stille and Suzuki-Miyaura cross-coupling reactions is explored, and a series of m- and p-terphenyl derivatives have been synthesized by conducting consecutive one-pot Stille and Suzuki-Miyaura cross-coupling reactions.