Combined isocyanide-based multi-component Ullmann-type reaction: an efficient access to novel nitrogen-containing pentacyclic compounds.

Dianat, Shima; Mahdavi, Mohammad; Moghimi, Setareh; Mouradzadegun, Arash; Shafiee, Abbas; Foroumadi, Alireza

Dianat, Shima; Mahdavi, Mohammad; Moghimi, Setareh; Mouradzadegun, Arash; Shafiee, Abbas; Foroumadi, Alireza.

Afiliação

Dianat S; Department of Chemistry, Faculty of Science, Shahid Chamran University, Ahvaz, Iran.
Mahdavi M; Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Moghimi S; Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Mouradzadegun A; Department of Chemistry, Faculty of Science, Shahid Chamran University, Ahvaz, Iran.
Shafiee A; Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Foroumadi A; Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran. aforoumadi@yahoo.com.

Mol Divers ; 19(4): 797-805, 2015 Nov.

Article em En | MEDLINE | ID: mdl-26232028

Assuntos

Cianetos/química; Quinolinas/síntese química; Ciclização; Estrutura Molecular; Nitrogênio/química; Quinolinas/química

Palavras-chave

2-Chloro-3-formyl-quinoline; Copper-mediated; Isocyanide-based multi-component reaction (IMCR); Polycyclic heterocycles; Ullmann-type reaction

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Cianetos Idioma: En Revista: Mol Divers Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Irã

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