ijms-logo

Journal Browser

Journal Browser

Transition Metal Catalysis: From Synthesis to Late-Stage Functionalization of Aromatics and Heterocycles

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Physical Chemistry and Chemical Physics".

Deadline for manuscript submissions: 31 August 2024 | Viewed by 724

Special Issue Editors


E-Mail Website
Guest Editor
Department of Chemistry and Industrial Chemistry, University of Pisa, 56124 Pisa, Italy
Interests: catalysis; organometallic chemistry; synthetic organic electrochemistry; synthetic photochemistry; isotope chemistry; radiochemistry; organic synthesis

E-Mail Website
Guest Editor
Department of Chemistry and Industrial Chemistry, University of Pisa, 56124 Pisa, Italy
Interests: transition metal-catalyzed reactions; (hetero)aromatic compounds; C–H bond activation; regioselectivity; cross-coupling; functional materials; bioactive compounds

Special Issue Information

Dear Colleagues,

Aromatic structures, specifically heterocycles, are ubiquitous key molecular entities included in many compounds with a broad range of applications, from pharmaceutical to material sciences. Transition metal catalysis (TMC) is a recognized and established branch of synthetic chemistry, largely exploited to carry out new and useful transformations. TMC has been extensively devoted to aromatics synthesis and late-stage functionalization (LSF) in this context. With the renaissance and exponential development of more sustainable protocols (photo-, electro-, flow, and mechanochemistry), TMC experienced a second boost within the last decade.

This Special Issue is dedicated solely to exploring recent advancements in the synthesis and utilization of transition metal complexes (TMCs) in conjunction with the catalytic construction and functionalization of aromatics and heteroaromatics. We aim to gather contributions from leading experts across academic and industrial sectors involved in this molecular field. We invite submissions of original research articles and critical reviews that highlight novel synthetic routes for TMCs, sustainable protocols, mechanistic investigations, and applications of TMC-catalyzed processes in aromatics’ synthesis, functionalization, and valorization. By showcasing the latest advancements and perspectives in this domain, we aim to foster cross-disciplinary collaborations and develop innovative solutions in molecular science.

Dr. Antonio Del Vecchio
Prof. Dr. Fabio Bellina
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. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. 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

  • transition metal catalysis
  • homogeneous catalysis
  • heterogeneous catalysis
  • cross-couplings
  • synthesis of aromatics and heteroaromatics
  • late-stage functionalization
  • photo-, electro-, flow, mechanochemistry
  • medicinal chemistry
  • material sciences
  • bioinorganic chemistry
  • industrial processes

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue polices can be found here.

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

10 pages, 2123 KiB  
Communication
Cobalt-Catalyzed Reduction of Aldehydes to Alcohols via the Hydroboration Reaction
by Dariusz Lewandowski and Grzegorz Hreczycho
Int. J. Mol. Sci. 2024, 25(14), 7894; https://doi.org/10.3390/ijms25147894 - 19 Jul 2024
Viewed by 523
Abstract
A method for the reduction of aldehydes with pinacolborane catalyzed by pincer cobalt complexes based on a triazine backbone is developed in this paper. The presented methodology allows for the transformation of several aldehydes bearing a wide range of electron-withdrawing and electron-donating groups [...] Read more.
A method for the reduction of aldehydes with pinacolborane catalyzed by pincer cobalt complexes based on a triazine backbone is developed in this paper. The presented methodology allows for the transformation of several aldehydes bearing a wide range of electron-withdrawing and electron-donating groups under mild conditions. The presented procedure allows for the direct one-step hydrolysis of the obtained intermediates to the corresponding primary alcohols. A plausible reaction mechanism is proposed. Full article
Show Figures

Graphical abstract

Back to TopTop