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Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions

Pyrans are one of the most significant skeletons of oxygen-containing heterocyclic molecules, which exhibit a broad spectrum of medicinal applications and are constituents of diverse natural product analogues. Various biological applications of these pyran analogues contributed to the growth advance...

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Detalles Bibliográficos
Autores principales: Maddila, Suresh, Kerru, Nagaraju, Jonnalagadda, Sreekantha Babu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571218/
https://www.ncbi.nlm.nih.gov/pubmed/36234888
http://dx.doi.org/10.3390/molecules27196347
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author Maddila, Suresh
Kerru, Nagaraju
Jonnalagadda, Sreekantha Babu
author_facet Maddila, Suresh
Kerru, Nagaraju
Jonnalagadda, Sreekantha Babu
author_sort Maddila, Suresh
collection PubMed
description Pyrans are one of the most significant skeletons of oxygen-containing heterocyclic molecules, which exhibit a broad spectrum of medicinal applications and are constituents of diverse natural product analogues. Various biological applications of these pyran analogues contributed to the growth advances in these oxygen-containing molecules. Green one-pot methodologies for synthesising these heterocyclic molecules have received significant attention. This review focuses on the recent developments in synthesising pyran ring derivatives using reusable catalysts and emphasises the multicomponent reaction strategies using green protocols. The advantages of the catalysts in terms of yields, reaction conditions, and recyclability are discussed.
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spelling pubmed-95712182022-10-17 Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions Maddila, Suresh Kerru, Nagaraju Jonnalagadda, Sreekantha Babu Molecules Review Pyrans are one of the most significant skeletons of oxygen-containing heterocyclic molecules, which exhibit a broad spectrum of medicinal applications and are constituents of diverse natural product analogues. Various biological applications of these pyran analogues contributed to the growth advances in these oxygen-containing molecules. Green one-pot methodologies for synthesising these heterocyclic molecules have received significant attention. This review focuses on the recent developments in synthesising pyran ring derivatives using reusable catalysts and emphasises the multicomponent reaction strategies using green protocols. The advantages of the catalysts in terms of yields, reaction conditions, and recyclability are discussed. MDPI 2022-09-26 /pmc/articles/PMC9571218/ /pubmed/36234888 http://dx.doi.org/10.3390/molecules27196347 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
Maddila, Suresh
Kerru, Nagaraju
Jonnalagadda, Sreekantha Babu
Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions
title Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions
title_full Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions
title_fullStr Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions
title_full_unstemmed Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions
title_short Recent Progress in the Multicomponent Synthesis of Pyran Derivatives by Sustainable Catalysts under Green Conditions
title_sort recent progress in the multicomponent synthesis of pyran derivatives by sustainable catalysts under green conditions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571218/
https://www.ncbi.nlm.nih.gov/pubmed/36234888
http://dx.doi.org/10.3390/molecules27196347
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