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      Visible-light-mediated synthesis of oxime esters via multicomponent reactions of aldehydes, aryl amines, and N-hydroxyphthalimide esters†

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          Oxime esters are useful scaffolds in many organic chemistry transformations. Herein, a novel visible-light-mediated three-component reaction for synthesis of oxime esters is reported. Aldehydes, aniline, and N-hydroxyphthalimide (NHPI) esters were used as substrates in this three-component reaction, and eosin Y was used as a crucial photocatalyst for the reaction. Wide ranges of aldehydes and NHPI esters were well tolerated in this reaction method, generating various oxime esters with high efficiency under mild reaction conditions. This visible-light-mediated methodology will be a promising approach to synthesize useful oxime esters in a single step.

          Abstract

          Practical and efficient visible-light-induced synthesis of oxime esters has been achieved via multicomponent reactions in the presence of catalytic eosin Y.

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          Organic Photoredox Catalysis.

          In this review, we highlight the use of organic photoredox catalysts in a myriad of synthetic transformations with a range of applications. This overview is arranged by catalyst class where the photophysics and electrochemical characteristics of each is discussed to underscore the differences and advantages to each type of single electron redox agent. We highlight both net reductive and oxidative as well as redox neutral transformations that can be accomplished using purely organic photoredox-active catalysts. An overview of the basic photophysics and electron transfer theory is presented in order to provide a comprehensive guide for employing this class of catalysts in photoredox manifolds.
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            Light-controlled tools.

            Spatial and temporal control over chemical and biological processes plays a key role in life, where the whole is often much more than the sum of its parts. Quite trivially, the molecules of a cell do not form a living system if they are only arranged in a random fashion. If we want to understand these relationships and especially the problems arising from malfunction, tools are necessary that allow us to design sophisticated experiments that address these questions. Highly valuable in this respect are external triggers that enable us to precisely determine where, when, and to what extent a process is started or stopped. Light is an ideal external trigger: It is highly selective and if applied correctly also harmless. It can be generated and manipulated with well-established techniques, and many ways exist to apply light to living systems--from cells to higher organisms. This Review will focus on developments over the last six years and includes discussions on the underlying technologies as well as their applications. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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              Pot economy and one-pot synthesis

              This review describes the importance and usefulness of pot-economy and one-pot reactions in current synthetic organic chemistry.
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                Author and article information

                Journal
                RSC Adv
                RSC Adv
                RA
                RSCACL
                RSC Advances
                The Royal Society of Chemistry
                2046-2069
                26 October 2023
                26 October 2023
                26 October 2023
                : 13
                : 45
                : 31346-31352
                Affiliations
                [a ] Department of Nuclear Medicine, Jeonbuk National University Medical School and Hospital Jeonju 54907 Republic of Korea hkkim717@ 123456jbnu.ac.kr
                [b ] Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital Jeonju 54907 Republic of Korea
                Author information
                https://orcid.org/0000-0001-7612-7049
                Article
                d3ra06737h
                10.1039/d3ra06737h
                10600831
                a44ec906-e160-4a62-b7b2-2dc36deec6d3
                This journal is © The Royal Society of Chemistry
                History
                : 4 October 2023
                : 21 October 2023
                Page count
                Pages: 7
                Funding
                Funded by: National Research Foundation of Korea, doi 10.13039/501100003725;
                Award ID: NRF/2021R1A2C1011204
                Funded by: Ministry of Science and ICT, South Korea, doi 10.13039/501100014188;
                Award ID: Unassigned
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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