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Ring forming transformations of ynamides via cycloaddition

Ynamides are N-alkyne compounds bearing an electron withdrawing group at the nitrogen atom. They offer unique pathways for the construction of versatile building blocks owing to their exceptional balance between reactivity and stability. Recently several studies have been reported that explore and i...

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Autores principales: Iftikhar, Ramsha, Mazhar, Aqsa, Iqbal, Muhammad Saqlain, Khan, Faiza Zahid, Askary, Syed Hassan, Sibtain, Hifza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072253/
https://www.ncbi.nlm.nih.gov/pubmed/37025669
http://dx.doi.org/10.1039/d3ra00139c
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author Iftikhar, Ramsha
Mazhar, Aqsa
Iqbal, Muhammad Saqlain
Khan, Faiza Zahid
Askary, Syed Hassan
Sibtain, Hifza
author_facet Iftikhar, Ramsha
Mazhar, Aqsa
Iqbal, Muhammad Saqlain
Khan, Faiza Zahid
Askary, Syed Hassan
Sibtain, Hifza
author_sort Iftikhar, Ramsha
collection PubMed
description Ynamides are N-alkyne compounds bearing an electron withdrawing group at the nitrogen atom. They offer unique pathways for the construction of versatile building blocks owing to their exceptional balance between reactivity and stability. Recently several studies have been reported that explore and illustrate the synthetic potential of ynamides and ynamide-derived advanced intermediates in cycloadditions with different reaction partners to yield heterocyclic cycloadducts of synthetic and pharmaceutical value. Cycloaddition reactions of ynamides are the facile and preferable routes for the construction of structural motifs having striking importance in synthetic, medicinal chemistry, and advanced materials. In this systematic review, we highlighted the recently reported novel transformations and synthetic applications that involved the cycloaddition reaction of ynamides. The scope along with the limitations of the transformations are discussed in detail.
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spelling pubmed-100722532023-04-05 Ring forming transformations of ynamides via cycloaddition Iftikhar, Ramsha Mazhar, Aqsa Iqbal, Muhammad Saqlain Khan, Faiza Zahid Askary, Syed Hassan Sibtain, Hifza RSC Adv Chemistry Ynamides are N-alkyne compounds bearing an electron withdrawing group at the nitrogen atom. They offer unique pathways for the construction of versatile building blocks owing to their exceptional balance between reactivity and stability. Recently several studies have been reported that explore and illustrate the synthetic potential of ynamides and ynamide-derived advanced intermediates in cycloadditions with different reaction partners to yield heterocyclic cycloadducts of synthetic and pharmaceutical value. Cycloaddition reactions of ynamides are the facile and preferable routes for the construction of structural motifs having striking importance in synthetic, medicinal chemistry, and advanced materials. In this systematic review, we highlighted the recently reported novel transformations and synthetic applications that involved the cycloaddition reaction of ynamides. The scope along with the limitations of the transformations are discussed in detail. The Royal Society of Chemistry 2023-04-04 /pmc/articles/PMC10072253/ /pubmed/37025669 http://dx.doi.org/10.1039/d3ra00139c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Iftikhar, Ramsha
Mazhar, Aqsa
Iqbal, Muhammad Saqlain
Khan, Faiza Zahid
Askary, Syed Hassan
Sibtain, Hifza
Ring forming transformations of ynamides via cycloaddition
title Ring forming transformations of ynamides via cycloaddition
title_full Ring forming transformations of ynamides via cycloaddition
title_fullStr Ring forming transformations of ynamides via cycloaddition
title_full_unstemmed Ring forming transformations of ynamides via cycloaddition
title_short Ring forming transformations of ynamides via cycloaddition
title_sort ring forming transformations of ynamides via cycloaddition
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072253/
https://www.ncbi.nlm.nih.gov/pubmed/37025669
http://dx.doi.org/10.1039/d3ra00139c
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