The reaction of diazomethane with chloroazirines: A new route to 1,2,3-triazines
โ Scribed by T.C. Gailagher; R.C. Storr
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 189 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The reaction of diazomethane with chloroazirines gives 1,2,3-triazines and chloromethylazirines.
๐ SIMILAR VOLUMES
The reaction of 1,2,4-triazinium salts with amides of acetoacetic acid yielding ,7,7a-hexahydro-6H-pyrrolo[3,2-e]-1,2,4-triazin-6-ones exemplifies the first direct to the 1,2,4-triazine ring based on the diaddition of bifunctional nucleophiles at C-5 and C-6.
## Abstract The reaction of 3โchloroโ6โphenylโ1,2,4โtriazine **1a** with carbon nucleophiles **2a๏ฃฟd** bearing a cyano substituent at a carbanionic center has been studied. In all reactions the formation of the corresponding 3โaminopyridazines **3a๏ฃฟd** takes place via ANRORC mechanism involving addi
## Abstract For Abstract see ChemInform Abstract in Full Text.