Reaction of ketooximes containing α-methylene group with chloramine-T followed by treatment with triethylamine leads to the formation of α-nitrosoolefins via α-nitrosochloride, which can react in situ intermolecularly with olefinic compounds to produce 5,6-dihydro-4H-1,2-oxazine derivatives in good yield.
|Number of pages||5|
|Journal||Journal of Heterocyclic Chemistry|
|Publication status||Published - 07-2005|
All Science Journal Classification (ASJC) codes
- Organic Chemistry