Abstract
β-Nitrostyrenes 1 react with stabilized nucleophiles to generate hydroximoyl chloride 2 after workup with ice cold concentrated hydrochloric acid. One-pot synthesis of five-membered carbocycles or cyclic ethers from the Michael addition of the carbon nucleophiles or alkoxides to the β-nitrostyrenes is reported.
| Original language | English |
|---|---|
| Pages (from-to) | 6419-6420 |
| Number of pages | 2 |
| Journal | Tetrahedron Letters |
| Volume | 38 |
| Issue number | 36 |
| DOIs | |
| Publication status | Published - 1997 Sept 8 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry