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Recent Advances in Photocatalytic Organic Synthesis

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

Deadline for manuscript submissions: closed (31 October 2023) | Viewed by 1185

Special Issue Editor


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Guest Editor
Natural Product & Medicinal Chemistry, CSIR-Indian Institute of Integrative Medicine, Jammu 180001, India
Interests: natural product chemistry; medicinal chemistry; photoredox catalysis

Special Issue Information

Dear Colleagues,

Recent years have seen the rapid emergence of photoredox catalysis as the use of visible light as a “reagent” in combination with catalysts has facilitated myriad efficient and selective chemical transformations which were otherwise deemed challenging to accomplish. Compared to other catalytic approaches, it offers the distinct advantage of enabling the activation of organic molecules under milder conditions using visible light as a sustainable energy source.

The main objective of this special issue is to highlight the recent advances in photoredox catalysis that have brought it to the forefront of research and development in synthetic organic chemistry, which will be critical for broader understanding and dissemination of this research field. This includes innovative applications, new reaction methodologies, novel catalyst design and fundamental physical aspects of photocatalysis.

Dr. Bhahwal Ali Shah
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 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

  • photoredox catalysis
  • visible light
  • organic synthesis
  • novel catalyst design
  • sustainable chemistry

Published Papers (1 paper)

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Research

15 pages, 1169 KiB  
Article
Hydroxy- and Hydro-Perfluoroalkylation of Styrenes by Controlling the Quenching Cycle of Eosin Y
by Haruko Shibata, Moeko Nakayama, Koto Tagami, Tadashi Kanbara and Tomoko Yajima
Molecules 2023, 28(22), 7577; https://doi.org/10.3390/molecules28227577 - 14 Nov 2023
Viewed by 937
Abstract
Fluoroalkyl compounds are widely used, underscoring a pressing need for the development of methods for their synthesis. However, reports on perfluoroalkylation to styrenes have been sparse. In this study, both hydroxy- and hydro-perfluoroalkylation of styrene were achieved using visible light reactions, catalyzed by [...] Read more.
Fluoroalkyl compounds are widely used, underscoring a pressing need for the development of methods for their synthesis. However, reports on perfluoroalkylation to styrenes have been sparse. In this study, both hydroxy- and hydro-perfluoroalkylation of styrene were achieved using visible light reactions, catalyzed by eosin Y, by selecting appropriate additives and controlling the eosin Y quenching cycle. These reactions are heavy-metal free, use water as the hydroxyl or hydrogen source, and employ inexpensive and readily available reagents. Full article
(This article belongs to the Special Issue Recent Advances in Photocatalytic Organic Synthesis)
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