| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5285375 | Tetrahedron Letters | 2006 | 4 Pages | 
Abstract
												We developed an efficient method for the synthesis of 3-substituted 2,3-dihydroquinolin-4-ones using a one-pot sequential multi-catalytic process: Pd-catalyzed allylic amination-thiazolium salt-catalyzed Stetter reaction cascade. Measurement of the initial rate of the developed sequential process revealed a significant increase in the reaction rate of the Stetter reaction in the presence of Pd(OAc)2 and AcOH·i-Pr2NEt, the constituents of the first Pd catalysis.
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											Authors
												Tetsuhiro Nemoto, Tomoaki Fukuda, Yasumasa Hamada, 
											