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.
Original language | English (US) |
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Pages (from-to) | 1195-1199 |
Number of pages | 5 |
Journal | Tetrahedron Letters |
Volume | 48 |
Issue number | 7 |
DOIs | |
State | Published - Feb 12 2007 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry