Phosphine- and water-promoted pentannulative aldol reaction†

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2346

Full metadata record

DC Field	Value	Language
dc.contributor.author	Satpathi, B.	-
dc.contributor.author	Dutta, L.	-
dc.contributor.author	Ramasastry, S.S.V.	-
dc.date.accessioned	2020-11-27T10:51:33Z	-
dc.date.available	2020-11-27T10:51:33Z	-
dc.date.issued	2019	-
dc.identifier.citation	Organic and Biomolecular Chemistry, 17(6),pp.1547-1551.	en_US
dc.identifier.other	https://doi.org/10.1039/C8OB03106A	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2019/ob/c8ob03106a#!divAbstract	-
dc.identifier.uri	http://hdl.handle.net/123456789/2346	-
dc.description.abstract	Herein, an efficient metal-free intramolecular aldol reaction for the synthesis of an unusual class of cyclopentanoids is described. The reaction of α-substituted dienones tethered with ketones in the presence of tributylphosphine and water provided aldols. The role of water was realised to be crucial for this transformation. Furthermore, isotopic labeling experiments provided vital information about the reaction mechanism.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Metal-free	en_US
dc.subject	Reaction	en_US
dc.subject	Efficient	en_US
dc.title	Phosphine- and water-promoted pentannulative aldol reaction†	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

Files in This Item:

File	Description	Size	Format
Need to add pdf.odt		8.63 kB	OpenDocument Text	View/Open