191-85-5Relevant articles and documents
Stereoselective tandem cascade furan cycloadditions
Criado, Alejandro,Vilas-Varela, Manuel,Cobas, Agustin,Perez, Dolores,Pena, Diego,Guitian, Enrique
, p. 12637 - 12649 (2013)
Oligofurans linked by a rigid tether undergo tandem cycloaddition reactions with high stereoselectivity. The reaction of bisfurans with dimethyl acetylenedicarboxylate (DMAD) involves tandem [4 + 2]/[4 + 2] cycloadditions in a pincer mode. The reaction of oligofurans with arynes involves stereoselective tandem [4 + 2]/[4 + 2] cycloaddition reactions in a domino mode. The corresponding aryne adducts have been transformed into extended perylene derivatives by deoxygenation and aromatization with HCl/EtOH.
Acid-promoted aromatization of perylene-based endoxides
Criado, Alejandro,Vilas-Varela, Manuel,Cobas, Agustín,Pérez, Dolores,Pe?a, Diego,Guitián, Enrique
, p. 1625 - 1632 (2016/11/13)
The aromatization of perylene-based endoxides by treatment with HCl and EtOH has been studied.
Organic electroluminescent device
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, (2008/06/13)
An electroluminescent device includes an anode, a cathode and at least one organic layer sandwiched between the anode and the cathode, the organic layer including a light-emitting layer which includes compound C1.