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Recent Progress in Synthesis and Bioactivity Studies of Heterocyclic Compounds

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organic Chemistry".

Deadline for manuscript submissions: closed (31 January 2023) | Viewed by 1418

Special Issue Editors


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Guest Editor
1. School of Pharmacy, Xinxiang University, Xinxiang 453000, China
2. Key Laboratory of Nano-Carbon Modified Film Technology Engineering of Henan Province, Xinxiang 453000, China
Interests: cycloadditions; synthesis; heterocycles; biologically active compounds; synthetic methodology

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Guest Editor
Department of Therapeutic Chemistry “Iuliu Hațieganu” University of Medicine and Pharmacy, 12 Ion Creangă Street, RO-400012 Cluj-Napoca, Romania
Interests: synthesis; heterocycles; azoles; antibiofilm; sortase A; antimicrobial; anti-inflammatory; ADMETOX; molecular docking

Special Issue Information

Dear Colleagues,

In this Special Issue, the aim is to report on recent advances in the use of heterocyclic scaffolds for the development of new bioactive molecules. Heterocyclic compounds play a remarkable role in the field of medicinal chemistry due to their correlation with various pharmacological properties. The molecules of most drugs used in therapy contain heterocyclic systems as active pharmacophores. At the same time, heterocycles could also influence other properties, such as lipophilicity, solubility, stability, and pharmacokinetics.

The multitude of methods available for the synthesis of various heterocycles offers many possibilities for the structural diversification and optimization of biologically active heterocyclic substances.

This Special Issue is dedicated but not limited to the presentation of results concerning the design, synthesis of novel heterocyclic compounds, and in silico/in vitro/in vivo assessment of their biological potential, mechanism of action, ADMETOX, etc.

Dr. Kaikai Wang
Dr. Smaranda Oniga
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • heterocycles
  • bioactivity
  • synthesis
  • molecular docking
  • mechanism of action

Published Papers (1 paper)

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Research

10 pages, 3714 KiB  
Article
Catalyst-Controlled Selectivity Switch in Three-Component Reaction: An NHC-Catalyzed Strategy for the Synthesis of δ-Lactone-Fused Spirobenzofuran-3-ones
by Zhanyong Wang, Ting Yang, Dongfang Liu, Rongxiang Chen, Nan Wang, Hong Liu, Jiarong Li, Kaikai Wang and Hongxin Liu
Molecules 2022, 27(18), 5952; https://doi.org/10.3390/molecules27185952 - 13 Sep 2022
Cited by 2 | Viewed by 1187
Abstract
An efficient, three-component reaction of aldehydes and benzofuran-3-ones was developed. This process provides a new approach for the preparation of synthetically and biologically important spirobenzofuran-3-one derivatives with moderate-to-good yields under mild conditions. A switch of intramolecular to intermolecular domino Michael–aldol–lactonization leading to differential [...] Read more.
An efficient, three-component reaction of aldehydes and benzofuran-3-ones was developed. This process provides a new approach for the preparation of synthetically and biologically important spirobenzofuran-3-one derivatives with moderate-to-good yields under mild conditions. A switch of intramolecular to intermolecular domino Michael–aldol–lactonization leading to differential product formation was achieved by different NHCs catalysis. Full article
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