Affiliations 

  • 1 Department of Chemistry, Government College University, Faisalabad, 38000, Pakistan
  • 2 Department of Chemistry, Government College University, Faisalabad, 38000, Pakistan. nasirrasool@gcuf.edu.pk
  • 3 Department of Chemistry, COMSATS Institute of Information Technology, University Road, Tobe Camp, Abbottabad, 22060, Pakistan
  • 4 The School of Chemistry & Chemical Engineering, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China
  • 5 Faculty of Industrial Sciences & Technology, University Malaysia Pahang, LebuhrayaTun, Razak, 26300, Kuantan, Pahang, Malaysia
  • 6 Deparment of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Science, University Putra Malaysia, 43400, Serdang, Selangor DarulEhsan, Malaysia. noorjahan@upm.edu.my
  • 7 Deparment of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Science, University Putra Malaysia, 43400, Serdang, Selangor DarulEhsan, Malaysia
Chem Cent J, 2018 Jul 17;12(1):84.
PMID: 30019193 DOI: 10.1186/s13065-018-0451-0

Abstract

A variety of imine derivatives have been synthesized via Suzuki cross coupling of N-(4-bromophenyl)-1-(3-bromothiophen-2-yl)methanimine with various arylboronic acids in moderate to good yields (58-72%). A wide range of electron donating and withdrawing functional groups were well tolerated in reaction conditions. To explore the structural properties, Density functional theory (DFT) investigations on all synthesized molecules (3a-3i) were performed. Conceptual DFT reactivity descriptors and molecular electrostatic potential analyses were performed by using B3LYP/6-31G(d,p) method to explore the reactivity and reacting sites of all derivatives (3a-3i).

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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