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Title
Japanese:Synthesis of Triphenylene Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Application to the Synthesis of Highly Fluorescent Triphenylene-Based Long Ladder Molecules. 
English:Synthesis of Triphenylene Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Application to the Synthesis of Highly Fluorescent Triphenylene-Based Long Ladder Molecules. 
Author
Japanese: Koichi Murayama, Yayoi Sawada, Keiichi Noguchi, Ken. Tanaka.  
English: Koichi Murayama, Yayoi Sawada, Keiichi Noguchi, Ken. Tanaka.  
Language English 
Journal/Book name
Japanese:Journal of Organic Chemistry 
English:Journal of Organic Chemistry 
Volume, Number, Page Vol. 78    No. 12    pp. 6202-6210
Published date 2013 
Publisher
Japanese:American Chemical Society 
English:American Chemical Society 
Conference name
Japanese: 
English: 
Conference site
Japanese: 
English: 
DOI https://doi.org/10.1021/jo4008892
Abstract The convenient synthesis of substituted triphenylenes and azatriphenylenes has been achieved by the cationic rhodium(I)/H8-BINAP or BINAP complex-catalyzed [2 + 2 + 2] cycloaddn. under mild conditions. E.g., in presence of [Rh(cod)2]BF4 and H8-BINAP, cycloaddn. of biaryl-linked diyne (I) and MeC竕。CCO2Et gave 89% triphenylene (II). Photophys. properties of representative triphenylenes and azatriphenylenes were examd., which revealed that azatriphenylenes showed higher fluorescence quantum yields than triphenylenes. This method was successfully applied to the synthesis of highly fluorescent triphenylene-based long ladder mols. [on SciFinder(R)]

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