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

green synthesis heterogeneous catalyst multicomponent reactions pyrans single-step synthesis

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
26 Sep 2022
Historique:
received: 14 08 2022
revised: 20 09 2022
accepted: 22 09 2022
entrez: 14 10 2022
pubmed: 15 10 2022
medline: 18 10 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 36234888
pii: molecules27196347
doi: 10.3390/molecules27196347
pmc: PMC9571218
pii:
doi:

Substances chimiques

Biological Products 0
Pyrans 0
Oxygen S88TT14065

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Références

Molecules. 2021 May 28;26(11):
pubmed: 34071629
J Colloid Interface Sci. 2018 Feb 1;511:392-401
pubmed: 29035802
Nat Prod Commun. 2011 Jun;6(6):841-3
pubmed: 21815422
Front Chem. 2021 Dec 22;9:800236
pubmed: 34993177
Molecules. 2020 Apr 20;25(8):
pubmed: 32326131
RSC Adv. 2022 May 12;12(22):14282-14298
pubmed: 35702657
Front Chem. 2021 Mar 31;9:638832
pubmed: 33869142
RSC Adv. 2021 Jul 5;11(38):23491-23505
pubmed: 35479799
RSC Adv. 2020 May 27;10(34):19803-19810
pubmed: 35520453
Arch Pharm (Weinheim). 2010 Feb;343(2):81-90
pubmed: 20077521
Bioorg Chem. 2021 Apr;109:104703
pubmed: 33609917
Mol Divers. 2020 May;24(2):345-354
pubmed: 31098860
Mol Divers. 2020 Nov;24(4):889-901
pubmed: 31598820
Chem Rev. 2014 Aug 27;114(16):8323-59
pubmed: 25032909
Org Biomol Chem. 2019 Aug 7;17(31):7270-7292
pubmed: 31313792

Auteurs

Suresh Maddila (S)

Department of Chemistry, GITAM School of Sciences, GITAM University, Visakhapatnam 530045, Andhra Pradesh, India.
School of Chemistry & Physics, University of KwaZulu-Natal, Westville Campus, Chiltern Hills, Durban 4000, South Africa.

Nagaraju Kerru (N)

School of Chemistry & Physics, University of KwaZulu-Natal, Westville Campus, Chiltern Hills, Durban 4000, South Africa.
Department of Chemistry, GITAM School of Science, GITAM University, Bengaluru Campus, Bengaluru 561203, Karnataka, India.

Sreekantha Babu Jonnalagadda (SB)

School of Chemistry & Physics, University of KwaZulu-Natal, Westville Campus, Chiltern Hills, Durban 4000, South Africa.

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Classifications MeSH