Novel Method for N-Alkylation of a Pyridone Ring.
β Scribed by E. N. Elizbarashvili; I. V. Lagvilava; Sh. A. Samsoniya
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 15 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
The first tertiary alkylations, alkoxyalkylations, and aldehyde enolate allylations are described proceeding with low catalyst loading (0.1 mol % to 5 mol %). The reactions proceed in short times, can be performed without solvent and under ambient conditions.
A Novel Strategy for N-Alkylation of Primary Amines. -The course of alkylation of aniline is dependent on the chain length of the alkyl bromide used. Under the reaction conditions (A) alkyl bromides with a number of carbon atoms β€ 4 give dialkylanilines exclusively, whereas alkylbromides with a num