ChemInform Abstract: Enzyme-Catalyzed Reactions. Part 32. Application of the Blaise Reaction: Stereoselective Synthesis of (4R)-tert-Butyl 3-Amino-4-trimethylsilyloxy-2-alkenoates from (R)-Cyanohydrins.
โ Scribed by J. SYED; S. FOERSTER; F. EFFENBERGER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Enzyme-Catalyzed Reactions. Part 26. Stereoselective Synthesis of (1R)-and (1R,2S)-1-Aryl-2-alkylamino Alcohols from (R)-Cyanohydrins. -Enantiomerically pure N-alkylated amino alcohols are prepared from cyanohydrins, accessible by (R)-oxynitrilase catalyzed addition of HCN to the appropriate aldehy
1999 stereochemistry stereochemistry (general, optical resolution) O 0030 24 -026 Synthesis of (-)-(4R,5R)-4,5-Bis [di-3'-(2',6'dimethoxypyridyl)phosphinomethyl] -2,2-dimethyl-1,3-dioxolane and Its Application in the Rh-Catalyzed Asymmetric Hydrogenation Reactions. -Asymmetric hydrogenations of a se