Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8384
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dc.contributor.authorBHOWMICK, ANINDITAen_US
dc.contributor.authorCHATTERJEE, ABHIJITen_US
dc.contributor.authorPATHAK, SIDHARTH S.en_US
dc.contributor.authorBHAT, RAMAKRISHNA G.en_US
dc.date.accessioned2024-01-02T05:31:14Z
dc.date.available2024-01-02T05:31:14Z
dc.date.issued2023-10en_US
dc.identifier.citationChemical Communications, 59(79), 11875-11878.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttps://doi.org/10.1039/D3CC02557Hen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8384
dc.description.abstractA straightforward and practical method has been developed to access α-substituted glutaric diesters from acrylates and aldehydes using visible light, with Eosin Y facilitating hydrogen atom transfer (HAT) and subsequent Giese-type addition. Also, sunlight has been successfully used as an alternative sustainable light source. The method has also been explored to access substituted 4,5-dihydro-2H-pyridazinones, which have potential biological and industrial applications. Comprehensive mechanistic investigations have been carried out.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectEstersen_US
dc.subject2023-DEC-WEEK3en_US
dc.subjectTOC-DEC-2023en_US
dc.subject2023en_US
dc.titleA visible light-driven direct synthesis of industrially relevant glutaric acid diesters from aldehydesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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