HBF 4 -catalyzed Mannich-type reaction of silyl enolates with aldimines took place smoothly in aqueous organic solvent to afford b-aminocarbonyl compounds in high yields. The HBF 4 -catalyzed Mannich-type reaction also proceeded smoothly in water without organic solvent in the presence of a surfacta
Mannich reactions catalyzed by perchloric acid in Triton X10 aqueous micelles
โ Scribed by Guo-ping Lu; Chun Cai
- Book ID
- 118427286
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 225 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1566-7367
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