Special Issue "Transition-Metal-Catalyzed Reactions in Organic Synthesis"

A special issue of Catalysts (ISSN 2073-4344).

Deadline for manuscript submissions: 30 September 2019.

Special Issue Editor

Guest Editor
Dr. Radim Hrdina Website E-Mail
Institute of Organic Chemistry, Justus Liebig University Giessen, Heinrich-Buff-Ring 17, 35392 Giessen, Germany
Interests: Organic synthesis and catalysis

Special Issue Information

Dear Colleagues,

Transition metal catalyzed reactions are fundamental for the synthesis of organic molecules. Homogeneous catalysis offers a very fast approach to new organic compounds, which are then tested for their desired properties, and thus helps to solve current health, environmental, energy storage and other problems. In this Special Issue, we would like to collect works that are focused on the development of new methodology in organic synthesis using transition metal catalysts, on the development of new transition metal complexes for catalysis of basic organic reactions, on the application of metal catalysts in the synthesis of special organic compounds, and on the development of artificial metallo-enzyme-like molecules.

This issue intends to cover all important processes in homogeneous catalysis, ranging from the synthesis of the smallest organic molecules as ammonia to complex natural products, using methods ranging from fundamental research to advanced applications. We look forward to compiling the best works of both academia and industry.

Dr. Radim Hrdina
Guest Editor

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 papers will be 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. Catalysts is an international peer-reviewed open access monthly 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 1600 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

  • Homogeneous catalysis
  • Transition metals
  • Synthesis of organic molecules
  • Catalyst development
  • Reaction mechanism
  • Organic synthetic methodology
  • Artificial metallo-enzymes

Published Papers (1 paper)

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Research

Open AccessFeature PaperArticle
Silver-Mediated Methoxylation of Aryl C(sp2)–H Bonds Directing by DMEDA
Catalysts 2019, 9(2), 171; https://doi.org/10.3390/catal9020171 - 12 Feb 2019
Abstract
The first example of silver-mediated phosphine-promoted methoxylation of aryl C(sp2)–H bonds with the commercially available reagent for the preparation of alkyl aryl ethers has been developed. This protocol is characterized by mild reaction conditions, broad substrate scope, and high regioselectivity. Full article
(This article belongs to the Special Issue Transition-Metal-Catalyzed Reactions in Organic Synthesis)
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Planned Papers

The below list represents only planned manuscripts. Some of these manuscripts have not been received by the Editorial Office yet. Papers submitted to MDPI journals are subject to peer-review.

Synthesis of Tri- and Disubstituted Fluorenols and Derivatives Thereof by Using Catalytic [2+2+2] Cyclotrimerization

Ilaria Caivano, Reinhard P. Kaiser, Florian Schnurrer, Jiří Mosinger, Ivana Císařová, David Nečas, and Martin Kotora

Abstract: A method for regioselective synthesis of 2,4-disubstituted fluorenols by using catalytic [2+2+2]cyclotrimerization of monosubstituted diynes with terminal alkynes was developed. The preferential formation of the 2,4-regioisomers was achieved in the presence of Cp*Ru(cod)Cl, whereas Rh-based catalysts tend to provide 3,4-regioisomers as the major products. The 2,4-disubstituted fluorenols were converted into the corresponding 9,9’-spirobifluorene derivatives and their structural and photophysical properties were evaluated.
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