| Literature DB >> 29277842 |
Tanay Kesharwani1, Krystal A Giraudy1, Jordan L Morgan1, Cory Kornman1, Abayomi D Olaitan1.
Abstract
Herein, we report the first synthesis of chlorinated benzo[b]selenophenes via environmentally friendly electrophilic chlorocyclization reaction using "table salt" as a source of "electrophilic chlorine" and ethanol as a solvent. In addition, the synthesis of diverse halogenated heterocycles, including 3-chloro, 3-bromo and 3-iodo thiophenes, selenophenes, and benzo[b]selenophenes was successfully accomplished under the same environmentally benign reaction conditions. This methodology has several advantages over other previously reported reactions as it employs simple starting compounds, an environmentally friendly solvent, ethanol, and non-toxic inorganic reagents under mild reaction conditions, resulting in the high product yields.Entities:
Keywords: Benzo[b]selenophene; Electrophilic halocyclization; Green Chemistry; Selenophene; Thiophene
Year: 2017 PMID: 29277842 PMCID: PMC5741090 DOI: 10.1016/j.tetlet.2017.01.007
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415