Green synthesis, in silico modeling, and biological evaluation of N-substituted (Z)-5-arylidene imidazolidine/thiazolidine-2,4-dione/4-thione derivatives catalyzed by Bu SO3H core–shell nanostructures-Reference-Cited by-同舟云学术

Green synthesis, in silico modeling, and biological evaluation of N-substituted (Z)-5-arylidene imidazolidine/thiazolidine-2,4-dione/4-thione derivatives catalyzed by Bu SO₃H core–shell nanostructures

Published:2024 Issue:32 Volume:14 Page:22916-22938
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Akhavan Malihe¹^ORCID,Esam Zohreh¹²,Mirshafa Atefeh³,Lotfi Maryam⁴,Pourmand Saeed⁵,Ashori Froug¹,Rabani Motahare¹,Ekbatani Golbahar¹,Tourani Saeed¹,Beheshti Reza¹,Keshavarzian Zahra¹,Ghanbarimasir Zahra⁶,Bekhradnia Ahmadreza¹^ORCID

Affiliation:

1. Pharmaceutical Sciences Research Center, Department of Medicinal Chemistry, Mazandaran University of Medical Sciences, Sari, Iran

2. Department of Medicinal Chemistry, School of Pharmacy, Babol University of Medical Sciences, Babol, Iran

3. Ramsar Campus, Mazandaran University of Medical Sciences, Ramsar, Iran

4. Department of Chemistry, NOVA, School of Science and Technology, Universidade NOVA de Lisboa, Portugal

5. Department of Chemical Engineering, Tabriz University of Chemical Engineering, Tabriz, Iran

6. Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran

Abstract

The newly designed magnetic nanocatalyst Fe3O4@CPTMS@guanidine–BuSO3H in a one-pot multicomponent reaction is reported to obtain N-substituted (Z)-5-arylidene imidazolidine/thiazolidine-2,4-dione/4-thione as a highly selective antiproliferation agent.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RA/D4RA03881A

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