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Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate
A selective and practical bromine–metal exchange on bromoheterocyclics bearing substituents with an acidic proton under non-cryogenic conditions was developed by a simple modification of an existing protocol. Our protocol of using a combination of i-PrMgCl and n-BuLi has not only solved the problem...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150384/ https://www.ncbi.nlm.nih.gov/pubmed/29137130 http://dx.doi.org/10.3390/molecules22111952 |
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author | Tian, Qingqiang Shang, Suqin Wang, Huajun Shi, Guoqiang Li, Zhiyao Yuan, Jianyong |
author_facet | Tian, Qingqiang Shang, Suqin Wang, Huajun Shi, Guoqiang Li, Zhiyao Yuan, Jianyong |
author_sort | Tian, Qingqiang |
collection | PubMed |
description | A selective and practical bromine–metal exchange on bromoheterocyclics bearing substituents with an acidic proton under non-cryogenic conditions was developed by a simple modification of an existing protocol. Our protocol of using a combination of i-PrMgCl and n-BuLi has not only solved the problem of intermolecular quenching that often occurred when using alkyl lithium alone as the reagent for halogen–lithium exchange, but also offered a highly selective method for performing bromo–metal exchange on dibrominated arene compounds through chelation effect. |
format | Online Article Text |
id | pubmed-6150384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61503842018-11-13 Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate Tian, Qingqiang Shang, Suqin Wang, Huajun Shi, Guoqiang Li, Zhiyao Yuan, Jianyong Molecules Article A selective and practical bromine–metal exchange on bromoheterocyclics bearing substituents with an acidic proton under non-cryogenic conditions was developed by a simple modification of an existing protocol. Our protocol of using a combination of i-PrMgCl and n-BuLi has not only solved the problem of intermolecular quenching that often occurred when using alkyl lithium alone as the reagent for halogen–lithium exchange, but also offered a highly selective method for performing bromo–metal exchange on dibrominated arene compounds through chelation effect. MDPI 2017-11-11 /pmc/articles/PMC6150384/ /pubmed/29137130 http://dx.doi.org/10.3390/molecules22111952 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tian, Qingqiang Shang, Suqin Wang, Huajun Shi, Guoqiang Li, Zhiyao Yuan, Jianyong Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate |
title | Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate |
title_full | Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate |
title_fullStr | Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate |
title_full_unstemmed | Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate |
title_short | Halogen–Metal Exchange on Bromoheterocyclics with Substituents Containing an Acidic Proton via Formation of a Magnesium Intermediate |
title_sort | halogen–metal exchange on bromoheterocyclics with substituents containing an acidic proton via formation of a magnesium intermediate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150384/ https://www.ncbi.nlm.nih.gov/pubmed/29137130 http://dx.doi.org/10.3390/molecules22111952 |
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