| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5282968 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The 1,4-elimination reaction of 1-amino-4-methoxy-(2Z)-alkenes is shown to proceed with high (1E,3E)-stereoselectivities to afford the corresponding 4-substituted-1-amino-1,3-dienes in good yield. The scope and stereochemical features of the synthetic method are described.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Eiji Tayama, Sayaka Sugai,