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Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach
A series of new quinazoline derivatives bearing a vinylic chloride group on the 2-position was prepared by using a consecutive S(RN)1 / E(RC)1 radical strategy.
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257244/ https://www.ncbi.nlm.nih.gov/pubmed/20428074 http://dx.doi.org/10.3390/molecules15042719 |
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author | Maillard-Boyer, Martine Castera-Ducros, Caroline Verhaeghe, Pierre Sifredi, France Rathelot, Pascal Vanelle, Patrice |
author_facet | Maillard-Boyer, Martine Castera-Ducros, Caroline Verhaeghe, Pierre Sifredi, France Rathelot, Pascal Vanelle, Patrice |
author_sort | Maillard-Boyer, Martine |
collection | PubMed |
description | A series of new quinazoline derivatives bearing a vinylic chloride group on the 2-position was prepared by using a consecutive S(RN)1 / E(RC)1 radical strategy. |
format | Online Article Text |
id | pubmed-6257244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62572442018-11-30 Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach Maillard-Boyer, Martine Castera-Ducros, Caroline Verhaeghe, Pierre Sifredi, France Rathelot, Pascal Vanelle, Patrice Molecules Article A series of new quinazoline derivatives bearing a vinylic chloride group on the 2-position was prepared by using a consecutive S(RN)1 / E(RC)1 radical strategy. Molecular Diversity Preservation International 2010-04-13 /pmc/articles/PMC6257244/ /pubmed/20428074 http://dx.doi.org/10.3390/molecules15042719 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Maillard-Boyer, Martine Castera-Ducros, Caroline Verhaeghe, Pierre Sifredi, France Rathelot, Pascal Vanelle, Patrice Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach |
title | Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach |
title_full | Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach |
title_fullStr | Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach |
title_full_unstemmed | Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach |
title_short | Access to Original Vinylic Chlorides in the Quinazoline Series via a Monoelectronic Transfer Reaction Approach |
title_sort | access to original vinylic chlorides in the quinazoline series via a monoelectronic transfer reaction approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257244/ https://www.ncbi.nlm.nih.gov/pubmed/20428074 http://dx.doi.org/10.3390/molecules15042719 |
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