Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications

Hiyama cross-coupling is a versatile reaction in synthetic organic chemistry for the construction of carbon–carbon bonds. It involves the coupling of organosilicons with organic halides using transition metal catalysts in good yields and high enantioselectivities. In recent years, hectic progress ha...

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Autores principales: Noor, Rida, Zahoor, Ameer Fawad, Irfan, Muhammad, Hussain, Syed Makhdoom, Ahmad, Sajjad, Irfan, Ali, Kotwica-Mojzych, Katarzyna, Mojzych, Mariusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458230/
https://www.ncbi.nlm.nih.gov/pubmed/36080422
http://dx.doi.org/10.3390/molecules27175654
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author Noor, Rida
Zahoor, Ameer Fawad
Irfan, Muhammad
Hussain, Syed Makhdoom
Ahmad, Sajjad
Irfan, Ali
Kotwica-Mojzych, Katarzyna
Mojzych, Mariusz
author_facet Noor, Rida
Zahoor, Ameer Fawad
Irfan, Muhammad
Hussain, Syed Makhdoom
Ahmad, Sajjad
Irfan, Ali
Kotwica-Mojzych, Katarzyna
Mojzych, Mariusz
author_sort Noor, Rida
collection PubMed
description Hiyama cross-coupling is a versatile reaction in synthetic organic chemistry for the construction of carbon–carbon bonds. It involves the coupling of organosilicons with organic halides using transition metal catalysts in good yields and high enantioselectivities. In recent years, hectic progress has been made by researchers toward the synthesis of diversified natural products and pharmaceutical drugs using the Hiyama coupling reaction. This review emphasizes the recent synthetic developments and applications of Hiyama cross-coupling.
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spelling pubmed-94582302022-09-09 Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications Noor, Rida Zahoor, Ameer Fawad Irfan, Muhammad Hussain, Syed Makhdoom Ahmad, Sajjad Irfan, Ali Kotwica-Mojzych, Katarzyna Mojzych, Mariusz Molecules Review Hiyama cross-coupling is a versatile reaction in synthetic organic chemistry for the construction of carbon–carbon bonds. It involves the coupling of organosilicons with organic halides using transition metal catalysts in good yields and high enantioselectivities. In recent years, hectic progress has been made by researchers toward the synthesis of diversified natural products and pharmaceutical drugs using the Hiyama coupling reaction. This review emphasizes the recent synthetic developments and applications of Hiyama cross-coupling. MDPI 2022-09-02 /pmc/articles/PMC9458230/ /pubmed/36080422 http://dx.doi.org/10.3390/molecules27175654 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Noor, Rida
Zahoor, Ameer Fawad
Irfan, Muhammad
Hussain, Syed Makhdoom
Ahmad, Sajjad
Irfan, Ali
Kotwica-Mojzych, Katarzyna
Mojzych, Mariusz
Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications
title Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications
title_full Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications
title_fullStr Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications
title_full_unstemmed Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications
title_short Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications
title_sort transition metal catalyzed hiyama cross-coupling: recent methodology developments and synthetic applications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458230/
https://www.ncbi.nlm.nih.gov/pubmed/36080422
http://dx.doi.org/10.3390/molecules27175654
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