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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/13947

Title: An intermolecular hydroamination of allenamides with arylamines catalyzed by cationic Au(I) salts
Authors: Hill, Anthony W.
Elsegood, Mark R.J.
Kimber, Marc C.
Issue Date: 2010
Publisher: © American Chemical Society
Citation: HILL, A.W., ELSEGOOD, M.R.J. and KIMBER, M.C., 2010. An intermolecular hydroamination of allenamides with arylamines catalyzed by cationic Au(I) salts. Journal of Organic Chemistry, 75 (15), pp. 5406 - 5409
Abstract: An intermolecular hydroamination of allenamides with arylamines has been achieved under mild Au(I) catalysis conditions delivering allylamino E-enamides stereoselectively and in high yield. The reaction is made possible via a convenient method for conjugated N-acyliminium formation.
Description: This article was published in the serial Journal of Organic Chemistry [© American Chemical Society]. The definitive version is available at: http://dx.doi.org/10.1021/jo101035n
Version: Accepted for publication
DOI: 10.1021/jo101035n
URI: https://dspace.lboro.ac.uk/2134/13947
Publisher Link: http://dx.doi.org/10.1021/jo101035n
ISSN: 0022-3263
Appears in Collections:Published Articles (Chemistry)

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