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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/13875
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dc.contributor.authorSarkar, Debayanen_US
dc.date.accessioned2024-07-05T12:49:26Z-
dc.date.available2024-07-05T12:49:26Z-
dc.date.issued2024-
dc.identifier.citationRoy, B., Kuila, P., Jha, S., & Sarkar, D. (2024). BF3·Et2O-assisted synthesis of sulfinylated spiro[5.5]trienones from biaryl ynones. Organic and Biomolecular Chemistry. Scopus. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85193066031&doi=10.1039%2fd3ob02010j&partnerID=40&md5=557a797cac206ff941baf21c5ccd52a5en_US
dc.identifier.issn1477-0520-
dc.identifier.otherEID(2-s2.0-85193066031)-
dc.identifier.urihttps://doi.org/10.1039/d3ob02010j-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/13875-
dc.description.abstractSulfinyls are valuable structural moieties used for developing synthetically new pharmaceuticals and agrochemicals. Herein, we disclose a straightforward synthesis of sulfinylated spiro[5.5]trienones proceeding via an unprecedented BF3·Et2O-promoted spirocyclization of biaryl ynones. The availability of relatively inexpensive BF3·Et2O to carry out transformations on a bulk scale along with its further application towards the synthesis of dibenzocyclohepten-5-ones delivers a unique opportunity to deploy it in various synthetic directions. © 2024 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceOrganic and Biomolecular Chemistryen_US
dc.titleBF3·Et2O-assisted synthesis of sulfinylated spiro[5.5]trienones from biaryl ynonesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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