Abstract
An equimolar reaction of the 2-diazo-1,2-diphenylethanone with 2-[(arylimino)methyl],phenols affords 2-[(arylimino)methyl]phenyl-2,2-diphenylacetates and 2-azetidinones. The products have been characterized on the basis of satisfactory spectral data. The regiochemistry of the reaction of hydroxyl and imino group towards diphenylketene, generated from thermal decomposition of the 2-diazo-1,2-diphenylethanone, has been observed to depend on the substituents on N-phenyl ring.
| Original language | English |
|---|---|
| Pages (from-to) | 212-213 |
| Number of pages | 2 |
| Journal | Letters in Organic Chemistry |
| Volume | 3 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 2006 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Organic Chemistry