Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115316
DC FieldValueLanguage
dc.contributorResearch Institute for Smart Energy-
dc.creatorSun, H-
dc.creatorGong, S-
dc.creatorZhang, H-
dc.creatorLiu, Y-
dc.creatorShi, LL-
dc.creatorZhu, Y-
dc.creatorXie, X-
dc.creatorLi, J-
dc.creatorWen, J-
dc.creatorGuan, Y, C-
dc.date.accessioned2025-09-19T03:24:03Z-
dc.date.available2025-09-19T03:24:03Z-
dc.identifier.urihttp://hdl.handle.net/10397/115316-
dc.language.isoenen_US
dc.publisherMolecular Diversity Preservation International (MDPI)en_US
dc.rights© 2025 by the authors. 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/).en_US
dc.rightsThe following publication Sun, H.-X., Gong, S.-X., Zhang, H.-Y., Liu, Y.-T., Shi, L.-L., Zhu, Y.-J., Xie, X.-M., Li, J.-J., Wen, J., Guan, Y.-C., Zhang, Z., Zhang, M., & Zhang, Y.-F. (2025). Research Progress on the Reaction of Carbon Dioxide with Hydrazones and Their Derivatives. Molecules, 30(9), 1987 is available at https://doi.org/10.3390/molecules30091987.en_US
dc.subjectCarbamatesen_US
dc.subjectCarbon dioxide (co2)en_US
dc.subjectCyclizationen_US
dc.subjectHydrazonesen_US
dc.subjectLactamizationen_US
dc.subjectUmpolung strategyen_US
dc.subjectCarbamic aciden_US
dc.subjectCarbon dioxideen_US
dc.subjectAmineen_US
dc.subjectCarbamic aciden_US
dc.subjectCarbamic acid derivativeen_US
dc.subjectCarbon dioxideen_US
dc.subjectHydrazone derivativeen_US
dc.subjectOrganic compounden_US
dc.subjectCarboxylationen_US
dc.subjectCyclizationen_US
dc.subjectDrug developmenten_US
dc.subjectOrganic synthesisen_US
dc.subjectPharmacologyen_US
dc.subjectReviewen_US
dc.subjectTherapyen_US
dc.titleResearch progress on the reaction of carbon dioxide with hydrazones and their derivativesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume30-
dc.identifier.issue9-
dc.identifier.doi10.3390/molecules30091987-
dcterms.abstractCO<inf>2</inf>, an abundant and renewable C1 source, presents significant potential for applications in organic synthesis. Hydrazones, recognized for their distinctive properties, exhibit high versatility in synthetic chemistry, facilitating numerous chemical transformations. Given their crucial roles in organic synthesis, the combination of CO<inf>2</inf> with hydrazones has garnered increasing research interest. This review provides a comprehensive summary of recent progress in reactions involving CO<inf>2</inf> and hydrazones or their derivatives. These include the coupling of amines and N-tosylhydrazones with CO<inf>2</inf>, the umpolung-mediated carboxylation of hydrazones/N-tosylhydrazones with CO<inf>2</inf>, the cyclization of hydrazones with CO<inf>2</inf>, and lactamization reactions incorporating N-tosylhydrazones and CO<inf>2</inf>. These transformations utilize the diverse reactivity of hydrazones and their derivatives to capture and convert CO<inf>2</inf>, generating valuable organic compounds with both academic and practical relevance. Additionally, the review examines the mechanisms underlying these reactions, offering critical insights for advancing research in this area.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMolecules, 2025, v. 30, no. 9, 1987-
dcterms.isPartOfMolecules-
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105004862002-
dc.identifier.pmid40363792-
dc.identifier.eissn1420-3049-
dc.identifier.artn1987-
dc.description.validate202509 bchy-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberCDCF_2024-2025en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis research was funded by the Natural Science Foundation of Sichuan Province (No. 2022NSFSC0200), the Sichuan Science and Technology Program (No. MZGC20240116), the Guangdong Basic and Applied Basic Research Foundation (No. 2022A1515111010), and the Shenzhen Science and Technology Program (No. RCBS20221008093229034). M. Zhang thanks the National Natural Science Foundation of China (62205276), the Hong Kong Research Grants Council (PolyU 15308324), and the PolyU Research Center for Organic Electronics (1-CE32) for providing financial support.en_US
dc.description.pubStatusPublisheden_US
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