An intermolecular hydroamination of allenamides with arylamines catalyzed by cationic Au(I) salts

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.

Bibliographic Details

Main Authors:	Anthony W. Hill, Mark Elsegood, Marc Kimber
Format:	Default Article
Published:	2010
Subjects:	Organic chemistry not elsewhere classified Other chemical sciences not elsewhere classified untagged Chemical Sciences not elsewhere classified Organic Chemistry
Online Access:	https://hdl.handle.net/2134/13947
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