Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6543
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dc.contributor.authorKHADE, VIKAS V.en_US
dc.contributor.authorTHUBE, ARCHANA S.en_US
dc.contributor.authorDHARPURE, PANKAJ D.en_US
dc.contributor.authorBHAT, RAMAKRISHNA G.en_US
dc.date.accessioned2022-01-31T11:26:09Z
dc.date.available2022-01-31T11:26:09Z
dc.date.issued2022-01en_US
dc.identifier.citationOrganic & Biomolecular Chemistry, 20(06), 1315-1319.en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttps://doi.org/10.1039/D1OB02154Ken_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6543
dc.description.abstractA visible light-mediated, metal-free, regioselective dihydrothionation of terminal aromatic as well as heteroaromatic alkynes has been achieved using Eosin Y as a photoredox catalyst at room temperature. The protocol gives direct access to different 1,3-dithiolanes under neutral and mild reaction conditions without the use of any base or additives. The electron-donating, electron-withdrawing and electron-deactivating groups tolerated the photocatalytic reaction conditions. The control experiments, cyclic voltammetry, and Stern–Volmer experiment were carried out to gain an insight into the mechanistic pathway. The protocol proved to be scalable at the gram level and also for practicality the deprotection of 1,3-dithiolanes has been demonstrated. The method uses clean energy under sustainable conditions.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2022-JAN-WEEK4en_US
dc.subjectTOC-JAN-2022en_US
dc.subject2022en_US
dc.titleDirect synthesis of 1,3-dithiolanes from terminal alkynes via visible light photoredox catalysisen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic & Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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