Organocatalytic β-Azidation of Enones Initiated by an Electron-Donor–Acceptor Complex

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2636

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DC Field	Value	Language
dc.contributor.author	Shirke, R.P.	-
dc.contributor.author	Ramasastry, S.S.V.	-
dc.date.accessioned	2020-12-04T04:59:14Z	-
dc.date.available	2020-12-04T04:59:14Z	-
dc.date.issued	2017	-
dc.identifier.citation	Organic Letters, 19(19), pp. 5482-5485	en_US
dc.identifier.other	https://doi.org/10.1021/acs.orglett.7b02861	-
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/acs.orglett.7b02861	-
dc.identifier.uri	http://hdl.handle.net/123456789/2636	-
dc.description.abstract	An operationally straightforward organocatalytic β-azidation of α,β-unsaturated ketones is described. Reaction of the Zhdankin azidoiodane with enones in the presence of a catalytic amount of an amine provides β-azido ketones via the formation of an electron-donor–acceptor complex. The application of this protocol is demonstrated through one-step elaborations leading to the synthesis of unprecedented classes of 1,2,3-triazoles.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Azides	en_US
dc.subject	Hydrocarbons	en_US
dc.subject	Organocatalytic	en_US
dc.subject	Electron-Donor–Acceptor	en_US
dc.title	Organocatalytic β-Azidation of Enones Initiated by an Electron-Donor–Acceptor Complex	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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