218769-45-0

Upstream product

• 533-58-4 2-Iodophenol 
• 637301-05-4 4-methoxybenzyl 2’-iodophenyl ether 
• 668971-66-2 ({2-[(4-methoxybenzyl)oxy]phenyl}ethynyl)(trimethyl)silane 
• 824-94-2 p-methoxybenzyl chloride 
• 209120-28-5 2-[(4-methoxyphenyl)methoxy]benzaldehyde 
• 90-02-8 salicylaldehyde 
• 2746-25-0 p-Methoxybenzyl bromide 

Relevant academic research and scientific papers

Visible light-induced radical addition/annulation to construct phenylsulfonyl-functionalized dihydrobenzofurans involving an intramolecular 1,5-hydrogen atom transfer process

A visible light-induced radical cascade reaction of 2-alkynylarylethers with sodium sulfinates was established for the synthesis of sulfonyl-functionalized dihydrobenzofurans, and an intramolecular 1,5-hydrogen atom transfer was involved in this transformation. This process provided an efficient and convenient C-C formation protocol for the construction of a dihydrobenzofuran ring. Various substituents on 2-alkynylarylethers and sodium sulfinates were tolerated in the reaction, and the corresponding products were obtained in moderate to good yields.

Synthesis of 2,3-Disubstituted Indoles and Benzofurans by the Tandem Reaction of Rhodium(II)-Catalyzed Intramolecular C-H Insertion and Oxygen-Mediated Oxidation

A highly effective and straightforward method to construct a wide range of functionalized 2,3-disubstituted indoles has been developed. The method involves the tandem reaction of rhodium(II)-catalyzed denitrogenative annulation of triazole-based benzyl an

ANTIBACTERIAL BENZOIC ACID DERIVATIVES

The invention provides antimicrobial agents and methods of using the agents for sterilization, sanitation, antisepsis, disinfection, and treatment of infections in mammals.