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Synthesis of novel antibacterial and antifungal dithiocarbamate-containing piperazine derivatives via re-engineering multicomponent approach.
Halimehjani, Azim Ziyaei; Dehghan, Faezeh; Tafakori, Vida; Amini, Elaheh; Hooshmand, Seyyed Emad; Nosood, Yazdanbkhsh Lotfi.
Afiliação
  • Halimehjani AZ; Faculty of Chemistry, Kharazmi University, 49 Mofateh St., 15719-14911, Tehran, Iran.
  • Dehghan F; Faculty of Chemistry, Kharazmi University, 49 Mofateh St., 15719-14911, Tehran, Iran.
  • Tafakori V; Department of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
  • Amini E; Department of Animal Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
  • Hooshmand SE; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Nosood YL; Faculty of Chemistry, Kharazmi University, 49 Mofateh St., 15719-14911, Tehran, Iran.
Heliyon ; 8(6): e09564, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35669544
ABSTRACT
A metal-free multicomponent synthetic route for the diverse preparation of dithiocarbamate-containing piperazine derivatives was developed through the C-N bond cleavage of DABCO ring. This multicomponent re-engineering approach proceeds via the reaction of amines, CS2 and DABCO salts in one pot. Various DABCO salts and secondary amines are tolerated well in this protocol to afford a broad spectrum of dithiocarbamate-containing piperazines in good to high yields. Then, the selected compounds have been deployed against some critical types of bacteria and fungi. A certain number of synthesized compounds revealed not only appropriate antibacterial activity as investigated by disc fusion and minimum inhibitory concentration methods against bacteria (Gram-positive and Gram-negative), but also depicted good to excellent antifungal activity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Heliyon Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Heliyon Ano de publicação: 2022 Tipo de documento: Article