An intermolecular hydroamination of allenamides with arylamines catalyzed by cationic Au(I) salts
journal contribution
posted on 2014-01-10, 13:15 authored by Anthony W. Hill, Mark ElsegoodMark Elsegood, Marc KimberMarc KimberAn 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.
History
School
- Science
Department
- Chemistry
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 - 5409Publisher
© American Chemical SocietyVersion
- AM (Accepted Manuscript)
Publication date
2010Notes
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/jo101035nISSN
0022-3263Publisher version
Language
- en
