A Friedländer route to 5,7-Diazapentacenes
A route to compounds with a 5,7-diazapentacene skeleton has been established involving a Friedländer reaction. A diaminodiketone 8 has been made by a novel method and reacted with cyclohexanone to prepare an octa-hydro-5,7-diazapentacene 7a and with tetralone to produce a dibenzotetrahydro-5,7-diaza...
Main Authors: | Lunchev, Andrey V., Hendrarta, Vincent Chandra, Jaggi, Aparna, Morris, Samuel Alexander, Ganguly, Rakesh, Chen, Xiaoxuan, Sun, Handong, Grimsdale, Andrew Clive |
---|---|
Other Authors: | School of Materials Science & Engineering |
Format: | Journal Article |
Language: | English |
Published: |
2018
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/87092 http://hdl.handle.net/10220/44254 |
Similar Items
-
Synthesis and electronic properties of novel 5,7-diazapentacene derivatives
by: Lunchev, Andrey V., et al.
Published: (2019) -
Recent progress in using pyrene-4,5-diketones and pyrene-4,5,9,10-tetraketones as building blocks to construct large acenes and heteroacenes
by: Jin, Pengcheng, et al.
Published: (2020) -
Synthesis, optical and electrochemical properties of isomeric dibenzophenanthroline derivatives
by: Ghosh, Animesh, et al.
Published: (2021) -
The Friedland–Hayman inequality and Caffarelli’s contraction theorem
by: Beck, T, et al.
Published: (2022) -
Synthetic route to quinolines via microwave irradiation assisted triflic acid-catalyzed friedländer annulation.
by: Hoeng, Murni.
Published: (2010)