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Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications

[Image: see text] Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows the corresponding arylation reactions to be performed under mild conditions. In the past decades, ac...

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Autores principales: Peng, Xiaopeng, Rahim, Abdur, Peng, Weijie, Jiang, Feng, Gu, Zhenhua, Wen, Shijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951228/
https://www.ncbi.nlm.nih.gov/pubmed/36649301
http://dx.doi.org/10.1021/acs.chemrev.2c00591
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author Peng, Xiaopeng
Rahim, Abdur
Peng, Weijie
Jiang, Feng
Gu, Zhenhua
Wen, Shijun
author_facet Peng, Xiaopeng
Rahim, Abdur
Peng, Weijie
Jiang, Feng
Gu, Zhenhua
Wen, Shijun
author_sort Peng, Xiaopeng
collection PubMed
description [Image: see text] Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows the corresponding arylation reactions to be performed under mild conditions. In the past decades, acyclic aryliodoniums are widely explored as arylation agents. However, the unmet need for acyclic aryliodoniums is the improvement of their notoriously low reaction economy because the coproduced aryl iodides during the arylation are often wasted. Cyclic aryliodoniums have their intrinsic advantage in terms of reaction economy, and they have started to receive considerable attention due to their valuable synthetic applications to initiate cascade reactions, which can enable the construction of complex structures, including polycycles with potential pharmaceutical and functional properties. Here, we are summarizing the recent advances made in the research field of cyclic aryliodoniums, including the nascent design of aryliodonium species and their synthetic applications. First, the general preparation of typical diphenyl iodoniums is described, followed by the construction of heterocyclic iodoniums and monoaryl iodoniums. Then, the initiated arylations coupled with subsequent domino reactions are summarized to construct polycycles. Meanwhile, the advances in cyclic aryliodoniums for building biaryls including axial atropisomers are discussed in a systematic manner. Finally, a very recent advance of cyclic aryliodoniums employed as halogen-bonding organocatalysts is described.
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spelling pubmed-99512282023-02-25 Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications Peng, Xiaopeng Rahim, Abdur Peng, Weijie Jiang, Feng Gu, Zhenhua Wen, Shijun Chem Rev [Image: see text] Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows the corresponding arylation reactions to be performed under mild conditions. In the past decades, acyclic aryliodoniums are widely explored as arylation agents. However, the unmet need for acyclic aryliodoniums is the improvement of their notoriously low reaction economy because the coproduced aryl iodides during the arylation are often wasted. Cyclic aryliodoniums have their intrinsic advantage in terms of reaction economy, and they have started to receive considerable attention due to their valuable synthetic applications to initiate cascade reactions, which can enable the construction of complex structures, including polycycles with potential pharmaceutical and functional properties. Here, we are summarizing the recent advances made in the research field of cyclic aryliodoniums, including the nascent design of aryliodonium species and their synthetic applications. First, the general preparation of typical diphenyl iodoniums is described, followed by the construction of heterocyclic iodoniums and monoaryl iodoniums. Then, the initiated arylations coupled with subsequent domino reactions are summarized to construct polycycles. Meanwhile, the advances in cyclic aryliodoniums for building biaryls including axial atropisomers are discussed in a systematic manner. Finally, a very recent advance of cyclic aryliodoniums employed as halogen-bonding organocatalysts is described. American Chemical Society 2023-01-17 /pmc/articles/PMC9951228/ /pubmed/36649301 http://dx.doi.org/10.1021/acs.chemrev.2c00591 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Peng, Xiaopeng
Rahim, Abdur
Peng, Weijie
Jiang, Feng
Gu, Zhenhua
Wen, Shijun
Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
title Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
title_full Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
title_fullStr Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
title_full_unstemmed Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
title_short Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
title_sort recent progress in cyclic aryliodonium chemistry: syntheses and applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951228/
https://www.ncbi.nlm.nih.gov/pubmed/36649301
http://dx.doi.org/10.1021/acs.chemrev.2c00591
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