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The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity

This review is an overview of the last ten years’ use of the Mizoroki–Heck coupling applied to 1,2- and 1,3-dienes. Since both these systems form π-allyl palladium intermediates in Pd(0) coupling, they show particular chemical behavior. Many examples of 1,2-dienes Heck reactions are presented. 1,2-D...

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Detalles Bibliográficos
Autores principales: Deagostino, Annamaria, Prandi, Cristina, Tabasso, Silvia, Venturello, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257322/
https://www.ncbi.nlm.nih.gov/pubmed/20428072
http://dx.doi.org/10.3390/molecules15042667
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author Deagostino, Annamaria
Prandi, Cristina
Tabasso, Silvia
Venturello, Paolo
author_facet Deagostino, Annamaria
Prandi, Cristina
Tabasso, Silvia
Venturello, Paolo
author_sort Deagostino, Annamaria
collection PubMed
description This review is an overview of the last ten years’ use of the Mizoroki–Heck coupling applied to 1,2- and 1,3-dienes. Since both these systems form π-allyl palladium intermediates in Pd(0) coupling, they show particular chemical behavior. Many examples of 1,2-dienes Heck reactions are presented. 1,2-Dienes are important substrates because of their high reactivity that makes them useful building blocks for the synthesis of biologically relevant structures.
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spelling pubmed-62573222018-11-30 The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity Deagostino, Annamaria Prandi, Cristina Tabasso, Silvia Venturello, Paolo Molecules Review This review is an overview of the last ten years’ use of the Mizoroki–Heck coupling applied to 1,2- and 1,3-dienes. Since both these systems form π-allyl palladium intermediates in Pd(0) coupling, they show particular chemical behavior. Many examples of 1,2-dienes Heck reactions are presented. 1,2-Dienes are important substrates because of their high reactivity that makes them useful building blocks for the synthesis of biologically relevant structures. Molecular Diversity Preservation International 2010-04-13 /pmc/articles/PMC6257322/ /pubmed/20428072 http://dx.doi.org/10.3390/molecules15042667 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 Review
Deagostino, Annamaria
Prandi, Cristina
Tabasso, Silvia
Venturello, Paolo
The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity
title The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity
title_full The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity
title_fullStr The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity
title_full_unstemmed The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity
title_short The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity
title_sort heck reaction applied to 1,3- and 1,2-unsaturated derivatives, a way towards molecular complexity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257322/
https://www.ncbi.nlm.nih.gov/pubmed/20428072
http://dx.doi.org/10.3390/molecules15042667
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