| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284138 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
The synthesized 1,3-dimethylated imidazolium-carbaldehydes serves as synthons for incorporating a permanently cationic imidazolium group into molecular framework. The utility of new synthon was demonstrated in a variety of reactions: Knoevenagel, Wittig, Schiff base formation, based-mediated electrophilic substitution, and oxidation, including synthesis of the natural product norzooanemonin.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mikhail Berezin, Samuel Achilefu,