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Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides

Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)(6) as the solid CO source, both cyclic and acyc...

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Autores principales: Peng, Jin-Bao, Wu, Fu-Peng, Xu, Cong, Qi, Xinxin, Ying, Jun, Wu, Xiao-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197950/
https://www.ncbi.nlm.nih.gov/pubmed/30321812
http://dx.doi.org/10.1016/j.isci.2018.09.024
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author Peng, Jin-Bao
Wu, Fu-Peng
Xu, Cong
Qi, Xinxin
Ying, Jun
Wu, Xiao-Feng
author_facet Peng, Jin-Bao
Wu, Fu-Peng
Xu, Cong
Qi, Xinxin
Ying, Jun
Wu, Xiao-Feng
author_sort Peng, Jin-Bao
collection PubMed
description Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)(6) as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well.
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spelling pubmed-61979502018-10-25 Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides Peng, Jin-Bao Wu, Fu-Peng Xu, Cong Qi, Xinxin Ying, Jun Wu, Xiao-Feng iScience Article Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)(6) as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well. Elsevier 2018-10-04 /pmc/articles/PMC6197950/ /pubmed/30321812 http://dx.doi.org/10.1016/j.isci.2018.09.024 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Peng, Jin-Bao
Wu, Fu-Peng
Xu, Cong
Qi, Xinxin
Ying, Jun
Wu, Xiao-Feng
Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
title Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
title_full Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
title_fullStr Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
title_full_unstemmed Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
title_short Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
title_sort nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197950/
https://www.ncbi.nlm.nih.gov/pubmed/30321812
http://dx.doi.org/10.1016/j.isci.2018.09.024
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