| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5283902 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
An enantioselective [3+2] annulation reaction of allenylstannane and α-imino ester was developed. Stille coupling of the resulting 4-stannyl dehydroproline gave optically active 4-arylated dehydroprolines in good yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Enantioselective three-component synthesis of 4-arylated dehydroprolines: [3+2] annulation of allenylstannane and α-imino ester](/preview/png/5283902.png "First Page Preview: Enantioselective three-component synthesis of 4-arylated dehydroprolines: [3+2] annulation of allenylstannane and α-imino ester")
Authors
Kohei Fuchibe, Rina Hatemata, Takahiko Akiyama,