Transition metal-catalyzed diastereoselective aldol reactions of prochiral ketones with methyl isocyanoacetate
โ Scribed by Vadim A. Soloshonok; Alexey D. Kacharov; Dimitry V. Avilov; Tamio Hayashi
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 279 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
During last two decades, a growing number of papers dealing with fluorine-containing amino acids have demonstrated the usefulness of these amino acids in the design of novel biologically active compounds as well as in the study of the biological chemistry. 2 A large number of fluoroamino acids have
Transition Metal/Base-Catalyzed Aldol Reactions of Isocyanoacetic Acid Derivatives with Prochiral Ketones, a Straightforward Approach to Stereochemically Defined ฮฒ,ฮฒ-Disubstituted-ฮฒ-hydroxy-. alpha.amino Acids. Scope and Limitations. -Methyl isocyanoacetate (II) undergoes aldol type reactions with