New conditions for the generation of dianions of carboxylic acids
✍ Scribed by Eva M. Brun; Isabel Casades; Salvador Gil; Ramón Mestres; Margarita Parra
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 242 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Lithium carboxylic acid enediolates are generated efficiently using lithium amides prepared from thienyllithium or butyllithium and either diethylamine, piperazine, N,N'-dibenzylethylenediarnine, N-benzylpiperazine or 1,3,3-trimethyl-6-azabicyclo[3.2.1 ]octane, even in catalytic amounts.
📜 SIMILAR VOLUMES
Seoul 131, Korea Reaction of carboxylic acids with equimolar amounts of alkyl chloroformate and triethylamine in the presence of a catalytic amount of 4-dimethylaminopyridine affords the corresponding esters in high yields without the formation of the symmetrical anhydride in most carboxylic acids.