Phosphine-catalysed denitrative rearomatising (3 + 2) annulation of α,β-ynones and 3-nitroindoles

dc.contributor.authorDutta, Lona
dc.contributor.authorChattopadhyay, Anwita
dc.contributor.authorYadava, Nisha
dc.contributor.authorRamasastry, S. S. V.
dc.date.accessioned2023-08-23T16:07:52Z
dc.date.available2023-08-23T16:07:52Z
dc.date.issued2022
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractWe describe a metal-free strategy to access various α-arylidene cyclopenta[b]indoles via phosphine-catalysed (3 + 2) annulation of α,β-ynones and 3-nitroindoles. For the first time, the rearomatisation of the indole nucleus was observed in such an annulative transformation. The method was extended to the synthesis of an antimalarial natural product, bruceolline E.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 21(4), 738- 742.en_US
dc.identifier.urihttps://doi.org/10.1039/d2ob02180c
dc.identifier.urihttp://hdl.handle.net/123456789/5107
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPhosphine-catalyseden_US
dc.subjectdenitrative rearomatisingen_US
dc.titlePhosphine-catalysed denitrative rearomatising (3 + 2) annulation of α,β-ynones and 3-nitroindolesen_US
dc.typeArticleen_US

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