| Literature DB >> 28271896 |
Og Soon Kim1, Jin Hyeok Jang1, Hyun Tae Kim1, Su Jin Han1, Gavin Chit Tsui2, Jung Min Joo1.
Abstract
The synthesis of indazoles from pyrazoles and internal alkynes is described. Instead of complex benzenoid compounds, readily available pyrazoles were used for the preparation of indazoles by reaction of the C-H bonds of the heterocyclic ring. Oxidative benzannulation was also applied to imidazoles, providing benzimidazoles. This convergent strategy enabled alteration of the photochemical properties of benzo-fused diazoles by varying the substituents at the benzene ring, thus leading to the development of tetraarylindazoles as new fluorophores.Entities:
Year: 2017 PMID: 28271896 DOI: 10.1021/acs.orglett.7b00410
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005