| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5267494 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
The regioselective hydroalkoxylation of homopropargyl tertiary ether catalyzed by Zeise's dimer was realized. The desired products were obtained in 61-95% yield with good regioselectivity. This methodology represents a valuable alternative to the aldol reaction or the oxa-Michael reaction to form prochiral tertiary β-hydroxy ketones.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ting Zhou, Guili Zhu, Xuan Huang, Bo Liu,