| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5289087 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Vinylketenes possessing a γ-heteroatom, on Staudinger cycloaddition reaction with imines, gave trans-3-vinyl-β-lactams in very good yields. The vinyl side chain stereoselectively adopts the Z-configuration in the transition state to stabilize the vinylketene and produces, exclusively, trans-3-vinyl-β-lactams.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Aarif L. Shaikh, Vedavati G. Puranik, A.R.A.S. Deshmukh,