23733-51-9

Upstream product

• 59024-26-9 1,2-C₂B₁₀H₁₀-1-CH₂CHCH₂S-2-C₆H₅ 
• 925-90-6 ethylmagnesium bromide 
• 71-43-2 benzene 

Downstream Products

• 71917-89-0 1,2-C₂B₁₀H₁₀-1-CHCHCH₃-2-C₆H₅ 

Relevant academic research and scientific papers

Photoarylation of Iodocarboranes with Unactivated (Hetero)Arenes: Facile Synthesis of 1,2-[(Hetero)Aryl]n-o-Carboranes (n=1,2) and o-Carborane-Fused Cyclics

Photoarylation of iodocarboranes with unactivated arenes/heteroarenes at room temperature has been achieved, for the first time, thus leading to the facile synthesis of a large variety of cage carbon mono(hetero)arylated and di(hetero)arylated o-carboranes. This work represents a clean, efficient, transition-metal-free, and cheap synthesis of functionalized carboranes, which has significant advantages over the known methods.