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- Photolysis of 1-aryl -1,2,3-triazoles; rearrangement via 1H-azirines. Glynn Mitchell, Charles W. Rees
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 413
- Lewis acid catalyzed [3 + 2] annulation of ketenimines with donor–acceptor cyclopropanes: an approach to 2-alkylidenepyrrolidine derivatives. Mateo Alajarin, Adrian Egea, Raul-Angel Orenes, Angel Vidal
, Org. Biomol. Chem.
, 2016
, 14
, 10275
- Microwave assisted Leimgruber–Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines. Jason Siu, Ian R. Baxendale, Steven V. Ley
, Org. Biomol. Chem.
, 2004
, 2
, 160
- Synthesis of biologically important, fluorescence active 5-hydroxy benzo[g]indoles through four-component domino condensations and their fluorescence “Turn-off” sensing of Fe(iii) ions. Subhendu Maity, Ashis Kundu, Animesh Pramanik
, RSC Adv.
, 2015
, 5
, 52852
- Reactions of some isoindoles with acetylenic esters. L. J. Kricka, J. M. Vernon
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 904
- The synthesis of 1-substituted 5-hydroxy-2-phenylindole derivatives from quinones. S. N. Betkerur, S. Siddappa
, J. Chem. Soc. C
, 1967
, 296
- High performance electrochromic devices based on a polyindole derivative, poly(1H-benzo[g]indole). Guangming Nie, Ling Wang, Changlong Liu
, J. Mater. Chem. C
, 2015
, 3
, 11318
- Synthesis of fused cyanopyrroles and spirocyclopropanes via addition of N-ylides to chalconimines. Siba Prasad Midya, Elumalai Gopi, Nishikant Satam, Irishi N. N. Namboothiri
, Org. Biomol. Chem.
, 2017
, 15
, 3616
- A benzoindole-cored building block for deep blue fluorescent materials: synthesis, photophysical properties, and applications in organic light-emitting diodes. Shanghui Ye, Congjin Wu, Pengfei Gu, Tai Xiang, Senyu Zhang, Tongtong Jing, Shi Wang, Xiaodi Yang, Yonghua Li, Wei Huang
, J. Mater. Chem. C
, 2020
, 8
, 16870
- Synthesis, characterization, and hole-transporting properties of benzotriazatruxene derivatives. Tianchai Chooppawa, Supawadee Namuangruk, Hiroshi M. Yamamoto, Vinich Promarak, Paitoon Rashatasakhon
, J. Mater. Chem. C
, 2019
, 7
, 15035