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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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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. |
format | Online Article Text |
id | pubmed-6197950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pengjinbao nickelcatalyzedcarbonylativesynthesisoffunctionalizedalkyliodides AT wufupeng nickelcatalyzedcarbonylativesynthesisoffunctionalizedalkyliodides AT xucong nickelcatalyzedcarbonylativesynthesisoffunctionalizedalkyliodides AT qixinxin nickelcatalyzedcarbonylativesynthesisoffunctionalizedalkyliodides AT yingjun nickelcatalyzedcarbonylativesynthesisoffunctionalizedalkyliodides AT wuxiaofeng nickelcatalyzedcarbonylativesynthesisoffunctionalizedalkyliodides |