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

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5107

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DC Field	Value	Language
dc.contributor.author	Dutta, Lona	-
dc.contributor.author	Chattopadhyay, Anwita	-
dc.contributor.author	Yadava, Nisha	-
dc.contributor.author	Ramasastry, S. S. V.	-
dc.date.accessioned	2023-08-23T16:07:52Z	-
dc.date.available	2023-08-23T16:07:52Z	-
dc.date.issued	2022	-
dc.identifier.citation	Organic and Biomolecular Chemistry, 21(4), 738- 742.	en_US
dc.identifier.uri	https://doi.org/10.1039/d2ob02180c	-
dc.identifier.uri	http://hdl.handle.net/123456789/5107	-
dc.description	Only IISER Mohali authors are available in the record.	en_US
dc.description.abstract	We 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.language.iso	en_US	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Phosphine-catalysed	en_US
dc.subject	denitrative rearomatising	en_US
dc.title	Phosphine-catalysed denitrative rearomatising (3 + 2) annulation of α,β-ynones and 3-nitroindoles	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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