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Direct synthesis of 1,3-dithiolanes from terminal alkynes via visible light photoredox catalysis

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dc.contributor.author KHADE, VIKAS V. en_US
dc.contributor.author THUBE, ARCHANA S. en_US
dc.contributor.author DHARPURE, PANKAJ D. en_US
dc.contributor.author BHAT, RAMAKRISHNA G. en_US
dc.date.accessioned 2022-01-31T11:26:09Z
dc.date.available 2022-01-31T11:26:09Z
dc.date.issued 2022-01 en_US
dc.identifier.citation Organic & Biomolecular Chemistry, 20(06), 1315-1319. en_US
dc.identifier.issn 1477-0539 en_US
dc.identifier.uri https://doi.org/10.1039/D1OB02154K en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6543
dc.description.abstract A 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.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.subject 2022-JAN-WEEK4 en_US
dc.subject TOC-JAN-2022 en_US
dc.subject 2022 en_US
dc.title Direct synthesis of 1,3-dithiolanes from terminal alkynes via visible light photoredox catalysis en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Organic & Biomolecular Chemistry en_US
dc.publication.originofpublisher Foreign en_US


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