| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5222689 | Tetrahedron | 2011 | 7 Pages | 
Abstract
												A gold (III)-catalyzed cascade reaction of propargyl acetates bearing an extra terminal alkyne (1) afforded γ-keto esters 3 and lactones 4. These products should be generated through allenyl ketone intermediate B via a 1,2-acyloxy cyclization/fragmentation/cycloisomerization/hydrolysis sequence. On the other hand, the cascade reaction of α-acetoxy ketones bearing terminal alkynes 5 afforded lactone 6 via allenyl ketone intermediate A. This reaction involves a [3,3]-sigmatropic acyloxy rearrangement/cycloisomerization/hydrolysis sequence.
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											Authors
												Taichi Kusakabe, Keisuke Kato, 
											