Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/16742
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dc.contributor.authorLenka, Bhabani Sankaren_US
dc.contributor.authorMishra, Rama Kanten_US
dc.contributor.authorSarkar, Debayanen_US
dc.date.accessioned2025-09-04T12:47:45Z-
dc.date.available2025-09-04T12:47:45Z-
dc.date.issued2025-
dc.identifier.citationLenka, B. S., Mishra, R. K., & Sarkar, D. (2025). Visible-Light-Induced Flavin Catalysis: A Green Route to Naphtho[2,1-b]furans via an o-(Naphtho)quinone Intermediate. Organic Letters, 27(29), 7738–7743. https://doi.org/10.1021/acs.orglett.5c00744en_US
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.otherEID(2-s2.0-105012418171)-
dc.identifier.urihttps://dx.doi.org/10.1021/acs.orglett.5c00744-
dc.identifier.urihttps://dspace.iiti.ac.in:8080/jspui/handle/123456789/16742-
dc.description.abstractA green and aerobic method for naphthofuran synthesis leverages riboflavin tetraacetate as a potent photocatalyst, accommodating diverse functional groups and a wide range of substrates. A comprehensive set of control experiments confirmed the involvement of o-(naphtho)quinone intermediates in the reaction mechanism, supporting the proposed catalytic pathway. This record is sourced from MEDLINE/PubMed, a database of the U.S. National Library of Medicineen_US
dc.language.isoenen_US
dc.sourceOrganic Lettersen_US
dc.subjectQuercetinen_US
dc.subjectRiboflavinen_US
dc.subjectQuercetinen_US
dc.subjectQuinone Derivativeen_US
dc.subjectRiboflavinen_US
dc.subjectArticleen_US
dc.subjectCatalysisen_US
dc.subjectDrug Analysisen_US
dc.subjectDrug Developmenten_US
dc.subjectReaction Analysisen_US
dc.subjectSynthesisen_US
dc.titleVisible-Light-Induced Flavin Catalysis: A Green Route to Naphtho[2,1-b]furans via an o-(Naphtho)quinone Intermediateen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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