1258425-91-0Relevant articles and documents
A 6π Azaelectrocyclization Strategy towards the 1,5,9-Triazacoronenes
Li, Jing,Shen, Guo-Dong,Sun, Hua-Ming,Sun, Yi-Xun,Wang, Xiao-Gang,Wei, Jun-Fa,Yang, Ming-Yu,Yang, Tian,Yang, Yi-Hui
, p. 1651 - 1656 (2020)
We present the instance of two aromatic double bonds and an imine double bond involved thermal 6π-azaelectrocyclization and, on this basis, a one-step synthesis of triazacoronenes (TACs) from triphenylene-1,5,9-triamines and aldehydes under nonacidic cond
1,5,9-triazacoronenes: A family of polycyclic heteroarenes synthesized by a threefold pictet-spengler reaction
Wei, Junfa,Han, Bo,Guo, Qiang,Shi, Xianying,Wang, Wenliang,Wei, Ni
supporting information; scheme or table, p. 8209 - 8213 (2011/02/22)
We are family: Triazacoronene derivatives have been synthesized in four steps from veratrole by using a threefold Pictet-Spengler reaction as the key step (see picture). They have good photophysical and electronical properties, thermal stability, and solu