Imidazoles from nitroallylic acetates and α-bromonitroalkenes with amidines: synthesis and trypanocidal activity studies
Author:
Affiliation:
1. Department of Chemistry
2. Indian Institute of Technology Bombay
3. Mumbai 400 076
4. India
5. Oswaldo Cruz Institute
6. FIOCRUZ
7. Rio de Janeiro
8. Brazil
9. Institute of Exact Sciences
10. Federal University of Minas Gerais
11. Belo Horizonte
Abstract
One-pot cascade reactions of amidines with nitroallylic acetates and α-bromonitroalkenes provide functionalized imidazoles that exhibit trypanocidal activity.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01444A
Reference130 articles.
1. Studies on the trypanocidal activity of semi-synthetic pyran[b-4,3]naphtho[1,2-d]imidazoles from β-lapachone
2. Trypanocidal activity of isolated naphthoquinones from Tabebuia and some heterocyclic derivatives: a review from an interdisciplinary study
3. Mitochondrial disruption and DNA fragmentation in Trypanosoma cruzi induced by naphthoimidazoles synthesized from β-lapachone
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