20904-86-3

Upstream product

• 849943-93-7 3,4-dihydronaphthalen-2-yl 4-methylbenzenesulfonate 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 105123-35-1 2,4,6-tris([1,1'-biphenyl]-4-yl)boroxine 
• 74626-11-2 3,4-dihydronaphthalen-2-yl N,N-dimethylcarbamate 

Relevant academic research and scientific papers

Bridged Stilbenes: AIEgens Designed via a Simple Strategy to Control the Non-radiative Decay Pathway

To broaden the application of aggregation-induced emission (AIE) luminogens (AIEgens), the design of novel small-molecular dyes that exhibit high fluorescence quantum yield (Φfl) in the solid state is required. Considering that the mechanism of

Nickel-catalyzed efficient and practical Suzuki-Miyaura coupling of alkenyl and aryl carbamates with aryl boroxines

(Figure Presented) Suzuki-Miyaura coupling of unactivated alkenyl carbamates Is described to construct polysubstituted olefins. The developed process is also suitable for heteroaromatic and even electron-rich aromatic carbamates.