| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274663 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
A combination of a catalyst derived from ferrous acetate and sodium thiophene-2-carboxylate efficiently promoted hydrosilylation of aromatic and aliphatic ketones to give the corresponding secondary alcohols in high yields with extremely high selectivity.
Graphical abstractThe hydrosilylation of ketones with ferrous acetate and thiophenecarboxylate as catalyst was realized to give the corresponding secondary alcohols in high yields and in high selectivity.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Akihiro Furuta, Hisao Nishiyama,