1356355-17-3Relevant academic research and scientific papers
Phenanthro[ b]-Fused BODIPYs through Tandem Suzuki and Oxidative Aromatic Couplings: Synthesis and Photophysical Properties
Miao, Wei,Feng, Yuanmei,Wu, Qinghua,Sheng, Wanle,Li, Mao,Liu, Qingyun,Hao, Erhong,Jiao, Lijuan
, p. 9693 - 9704 (2019)
A new synthetic method to build phenanthrene-fused boron dipyrromethenes (BODIPYs) through tandem Suzuki couplings on readily available 2,3,5,6-tetrabromoBODIPYs, followed by an intramolecular oxidative aromatic coupling mediated by iron(III) chloride is
Facile synthesis of biphenyl-fused BODIPY and its property
Hayashi, Yosuke,Obata, Naoki,Tamaru, Masatomo,Yamaguchi, Shigeru,Matsuo, Yutaka,Saeki, Akinori,Seki, Shu,Kureishi, Yuka,Saito, Shohei,Yamaguchi, Shigehiro,Shinokubo, Hiroshi
supporting information; experimental part, p. 866 - 869 (2012/05/05)
A biphenyl-fused BODIPY was synthesized through a facile oxidative cyclization of peripheral aryl-substituents at the β-position of the BODIPY unit. The extended π-system of the fused BODIPY induces near-infrared (NIR) absorption and strong π - π interact
