Abstract
A three-component strategy starting from isocyanides allows a straightforward synthesis of five-membered ring heterocycles. New cascades were developed involving the addition of a nitrogenated nucleophile-an azide or a tetrazole-on isocyanide dibromides, an electrocyclization, and a Suzuki coupling, which afford new accesses to tetrazole and triazole scaffolds.(Figure Presented)
| Original language | English |
|---|---|
| Pages (from-to) | 1261-1263 |
| Number of pages | 3 |
| Journal | Organic Letters |
| Volume | 13 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 4 Mar 2011 |
| Externally published | Yes |
Fingerprint
Dive into the research topics of 'Three-component strategy toward 5-membered heterocycles from isocyanide dibromides.'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver