The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins

This review covers palladium-catalyzed typical Mizoroki–Heck cross-coupling reactions of aryl halides with in situ generated alkenes, by following a typical Heck coupling mechanism to form substituted olefins unlike direct cross-coupling of alkenes with aryl halides in Heck olefination. These reacti...

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Autores principales: Koranne, Anushka, Turakhia, Shrishty, Jha, Vikesh Kumar, Gupta, Sangeeta, Ravi, Rangnath, Mishra, Abhijeet, Aggarwal, Anil K., Jha, Chandan Kumar, Dheer, Neelu, Jha, Abadh Kishor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10367967/
https://www.ncbi.nlm.nih.gov/pubmed/37497097
http://dx.doi.org/10.1039/d3ra03533f
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author Koranne, Anushka
Turakhia, Shrishty
Jha, Vikesh Kumar
Gupta, Sangeeta
Ravi, Rangnath
Mishra, Abhijeet
Aggarwal, Anil K.
Jha, Chandan Kumar
Dheer, Neelu
Jha, Abadh Kishor
author_facet Koranne, Anushka
Turakhia, Shrishty
Jha, Vikesh Kumar
Gupta, Sangeeta
Ravi, Rangnath
Mishra, Abhijeet
Aggarwal, Anil K.
Jha, Chandan Kumar
Dheer, Neelu
Jha, Abadh Kishor
author_sort Koranne, Anushka
collection PubMed
description This review covers palladium-catalyzed typical Mizoroki–Heck cross-coupling reactions of aryl halides with in situ generated alkenes, by following a typical Heck coupling mechanism to form substituted olefins unlike direct cross-coupling of alkenes with aryl halides in Heck olefination. These reactions solve the issue of alkenes undergoing polymerization at high temperatures and increase reaction efficiency by reducing the reaction time and purification steps.
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spelling pubmed-103679672023-07-26 The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins Koranne, Anushka Turakhia, Shrishty Jha, Vikesh Kumar Gupta, Sangeeta Ravi, Rangnath Mishra, Abhijeet Aggarwal, Anil K. Jha, Chandan Kumar Dheer, Neelu Jha, Abadh Kishor RSC Adv Chemistry This review covers palladium-catalyzed typical Mizoroki–Heck cross-coupling reactions of aryl halides with in situ generated alkenes, by following a typical Heck coupling mechanism to form substituted olefins unlike direct cross-coupling of alkenes with aryl halides in Heck olefination. These reactions solve the issue of alkenes undergoing polymerization at high temperatures and increase reaction efficiency by reducing the reaction time and purification steps. The Royal Society of Chemistry 2023-07-25 /pmc/articles/PMC10367967/ /pubmed/37497097 http://dx.doi.org/10.1039/d3ra03533f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Koranne, Anushka
Turakhia, Shrishty
Jha, Vikesh Kumar
Gupta, Sangeeta
Ravi, Rangnath
Mishra, Abhijeet
Aggarwal, Anil K.
Jha, Chandan Kumar
Dheer, Neelu
Jha, Abadh Kishor
The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
title The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
title_full The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
title_fullStr The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
title_full_unstemmed The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
title_short The Mizoroki–Heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
title_sort mizoroki–heck reaction between in situ generated alkenes and aryl halides: cross-coupling route to substituted olefins
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10367967/
https://www.ncbi.nlm.nih.gov/pubmed/37497097
http://dx.doi.org/10.1039/d3ra03533f
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