Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10399
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dc.contributor.authorMEHER, KAJAL B.en_US
dc.contributor.authorBANKAR, ONKAR S.en_US
dc.contributor.authorMUKHERJEE, HRISHIKen_US
dc.contributor.authorBHAT, RAMAKRISHNA G.en_US
dc.date.accessioned2025-09-16T06:14:10Z-
dc.date.available2025-09-16T06:14:10Z-
dc.date.issued2025-08en_US
dc.identifier.citationChemistry – An Asian Journalen_US
dc.identifier.issn1861-471Xen_US
dc.identifier.issn1861-4728en_US
dc.identifier.urihttps://doi.org/10.1002/asia.202500702en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10399-
dc.description.abstractDirhodium(II)-catalyzed regio-divergent intramolecular rearrangement of oxonium and sulfonium ylides, generated from diazo arylidene succinimides (DAS), has been achieved at room temperature. Allyloxy-substituted DAS derivatives were strategically designed and synthesized to explore their reactivity under metal catalysis. The transformation is proposed to proceed via oxonium ylide intermediate, followed by [1,2]- and [1,4]-shifts, leading to the chromene framework. This strategy was further extended to thioallyl-substituted DASs to access thiochromenes under mild reaction conditions. For the first time, intramolecular rearrangement has been explored on DAS derivatives to synthesize bioactive chromene and thiochromene scaffolds.en_US
dc.language.isoenen_US
dc.publisherWleyen_US
dc.subject[1,2]/[1,4]-shiften_US
dc.subjectChromenesen_US
dc.subjectDiazo arylidene succinimideen_US
dc.subjectRegiodivergenten_US
dc.subjectThiochromenesen_US
dc.subject2025-SEP-WEEK1en_US
dc.subjectTOC-SEP-2025en_US
dc.subject2025en_US
dc.titleOxonium/Sulfonium Ylide Rearrangements to Access Chromenes and Thiochromenes: Concerted or Stepwise Pathway?en_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry – An Asian Journalen_US
dc.publication.originofpublisherForeignen_US
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